Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:100950427-100950709 | Common:10; Rare:119 | ||||
chr8:101205165-101205416 | Rare:61 | ||||
chr8:101205546-101205880 | Common:4; Rare:108 | ||||
chr8:102238660-102239004 | Common:7; Rare:149; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr8:102412656-102412895 | Common:1; Rare:58 | ||||
chr8:102864153-102864290 | Rare:61 | ||||
chr8:102864403-102864540 | Common:1; Rare:50 | ||||
chr8:103020932-103021132 | Rare:62 | ||||
chr8:103298708-103298956 | Common:2; Rare:59 | ||||
chr8:103415007-103415497 | Common:6; Rare:244 | ||||
chr8:105319270-105319561 | Rare:63 | ||||
chr8:106657540-106657969 | Common:5; Rare:123 | ||||
chr8:107497356-107497718 | Common:2; Rare:98 | ||||
chr8:108248670-108248837 | Rare:73 | ||||
chr8:108443472-108443661 | Common:2; Rare:84 |