| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:235866876-235867116 | Common:3; Rare:71 | ||||
| chr1:236065047-236065348 | Common:2; Rare:115; Clinvar (pathogenic):1 | ||||
| chr1:236281956-236282258 | Common:6; Rare:90 | ||||
| chr1:236523834-236524053 | Common:3; Rare:56 | ||||
| chr1:236604486-236604645 | Common:4; Rare:45 | ||||
| chr1:236795080-236795446 | Common:6; Rare:149; Clinvar:3 | ||||
| chr1:241848121-241848232 | Rare:21 | ||||
| chr1:243255045-243255432 | Common:1; Rare:93 | ||||
| chr1:243255752-243256136 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:243487756-243487821 | Common:1; Rare:17 | ||||
| chr1:244835561-244835736 | Common:2; Rare:74; Clinvar (benign):4 | ||||
| chr1:244864147-244864614 | Rare:157; Clinvar:1; Clinvar (benign):3 | ||||
| chr1:244970212-244970433 | Common:4; Rare:107 | ||||
| chr1:246507241-246507375 | Common:1; Rare:53 | ||||
| chr1:246566204-246566587 | Common:1; Rare:125 |