| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:778633-778820 | Common:2; Rare:75 | ||||
| chr1:827515-827679 | Common:1; Rare:71 | ||||
| chr1:2174472-2174499 | Common:1; Rare:7 | ||||
| chr1:2554155-2554278 | Rare:35 | ||||
| chr1:9182135-9182235 | Rare:24 | ||||
| chr1:16644644-16644803 | Common:1; Rare:3 | ||||
| chr1:19219468-19219554 | Rare:24 | ||||
| chr1:21827861-21828153 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:21831461-21831797 | Common:2; Rare:106; Clinvar:3; Clinvar (benign):2 | ||||
| chr1:21850039-21850502 | Common:4; Rare:153; Clinvar:9; Clinvar (benign):1 | ||||
| chr1:21855514-21855913 | Common:4; Rare:135; Clinvar:9; Clinvar (benign):5 | ||||
| chr1:21857014-21857386 | Common:1; Rare:118; Clinvar:7; Clinvar (benign):3 | ||||
| chr1:21859564-21860003 | Common:2; Rare:141; Clinvar:4 | ||||
| chr1:21872618-21873115 | Common:5; Rare:149; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:21876227-21876656 | Common:2; Rare:153; Clinvar:11; Clinvar (benign):2 |