| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:154983110-154983433 | Common:2; Rare:69; Clinvar (benign):2 | ||||
| chr1:155033723-155033842 | Rare:19 | ||||
| chr1:155050584-155050642 | Rare:15 | ||||
| chr1:155051118-155051349 | Common:1; Rare:78 | ||||
| chr1:155063946-155064113 | Common:1; Rare:50 | ||||
| chr1:155084932-155085034 | Common:2; Rare:30 | ||||
| chr1:155127728-155127937 | Common:1; Rare:43 | ||||
| chr1:155135165-155135398 | Rare:48 | ||||
| chr1:155135707-155135909 | Common:3; Rare:87 | ||||
| chr1:155140489-155140639 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:155172820-155173389 | Common:4; Rare:186 | ||||
| chr1:155193113-155193467 | Common:1; Rare:73 | ||||
| chr1:155196265-155196451 | Common:2; Rare:27 | ||||
| chr1:155207890-155208058 | Rare:41 | ||||
| chr1:155208206-155208459 | Rare:46 |