| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:155934354-155934663 | Common:2; Rare:114 | ||||
| chr1:155978540-155978640 | Rare:24 | ||||
| chr1:156020856-156021024 | Rare:58 | ||||
| chr1:156053708-156053922 | Rare:59 | ||||
| chr1:156054615-156054887 | Common:3; Rare:77 | ||||
| chr1:156114511-156114901 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):4 | ||||
| chr1:156193810-156194129 | Common:3; Rare:80 | ||||
| chr1:156212875-156213078 | Common:1; Rare:65 | ||||
| chr1:156213222-156213370 | Common:2; Rare:34 | ||||
| chr1:156282780-156283025 | Common:2; Rare:62 | ||||
| chr1:156338147-156338583 | Common:2; Rare:157 | ||||
| chr1:156591728-156591897 | Common:4; Rare:88 | ||||
| chr1:156601422-156601513 | Common:1; Rare:36 | ||||
| chr1:156641997-156642203 | Rare:54 | ||||
| chr1:156677397-156677515 | Rare:23 |