Variant position | Gene symbol |
---|---|
Exon | MYO19, MYH8, MYH3, ENSSSCG00000038539, MYH4, ENSSSCG00000007733, ENSSSCG00000033141, CCT6A, ZNF713, ENSSSCG00000036685, ITAGM, ZNF646, SETD1A, STX4, RNF40, HSD3B7, CCDC189, TAMALIN, EPHB2, ELOA and OTOP1. |
Intron | DHRS11, MYH13, MYH8, MYH3, MYH4, UNC5D, SLC22A11, ENSSSCG00000033141, RARB, ENSSSCG00000047703, MMS19, UNC5D, SLC22A11, KCTD7, ENSSSCG00000007733, ZNF713, SEPTIN14, CCT6A, SETDA1, ZNF629, RNF40, CCDC189, DEDD, NIT1, TAMALIN, EPHB2, TEX46, LUZP1, LYPLA2, CNR2, FUCA1, PAPLAN, PDLIM5 and RAPGEF5. |
Upstream | MYH3, HSD3B7, SETD1A, ORAI3, RNF40, PFDN2, CNR2, CLIC4, UBASH3B, LOC100514433, ENSSSCG00000049720, LOC106509673, ENSSSCG00000018553, ENSSSCG00000033141, SUMF2 and ENSSSCG00000007735 |
5′ UTR | ZNF713, BCKDK, ZNF629, RNF40, CNR2, ENSSSCG00000036685 and ENSSSCG00000007733. |
Downstream | DHRS11, ADPRM, KCTD7, ZNF713, PRSS53, VKORC1, HSD3B7, STX1B, SETD1A, RNF40, ZNF629, PHKG2, ROCK2, SLC66A3, NIT1, EPHB2, ENSSSCG00000047341, ENSSSCG00000018553, ENSSSCG00000033141 and ENSSSCG00000027233 |
3′ UTR | ZNHIT3, MYO19, DHRS11, KCTD7, CCT6A, ZNF713, STX1B, HSD3B7, ORAI3, ZNF629, PHKG2 and EPHB2. |