| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161046237-161046388 | Rare:28 | ||||
| chr1:161069776-161070177 | Rare:53 | ||||
| chr1:161098264-161098469 | Common:2; Rare:45 | ||||
| chr1:161117455-161117660 | Rare:42 | ||||
| chr1:161117710-161117825 | Common:1; Rare:28 | ||||
| chr1:161117956-161118197 | Rare:123 | ||||
| chr1:161132538-161133171 | Common:3; Rare:153 | ||||
| chr1:161153686-161154089 | Common:1; Rare:115; Clinvar (pathogenic):1 | ||||
| chr1:161159389-161159572 | Common:1; Rare:57 | ||||
| chr1:161166152-161166770 | Common:4; Rare:147; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:161177000-161177244 | Common:1; Rare:66 | ||||
| chr1:161177373-161177772 | Common:1; Rare:104 | ||||
| chr1:161202127-161202517 | Common:3; Rare:121; Clinvar:5; Clinvar (benign):10 | ||||
| chr1:161202667-161202759 | Common:2; Rare:11 | ||||
| chr1:161225630-161226283 | Common:13; Rare:113 |