Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:96799424-96799778 | Common:3; Rare:71 | ||||
chr1:97529950-97529998 | Rare:11 | ||||
chr1:97533125-97533239 | Common:3; Rare:25 | ||||
chr1:98028961-98029082 | Common:1; Rare:17 | ||||
chr1:108696046-108696367 | Common:1; Rare:59 | ||||
chr1:108925335-108925544 | Common:2; Rare:25 | ||||
chr1:109409769-109409985 | Rare:45 | ||||
chr1:109424052-109424149 | Common:1; Rare:16 | ||||
chr1:109592050-109592448 | Rare:85 | ||||
chr1:110361334-110361612 | Rare:44 | ||||
chr1:113561047-113561193 | Common:1; Rare:21 | ||||
chr1:114707942-114708157 | Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
chr1:117366566-117366850 | Common:1; Rare:78 | ||||
chr1:120415773-120415857 | Common:2; Rare:18 | ||||
chr1:144551928-144552215 | Rare:94 |