| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:117060067-117060360 | Common:6; Rare:75 | ||||
| chr1:117929568-117929806 | Common:4; Rare:71 | ||||
| chr1:119140644-119140768 | Common:1; Rare:37 | ||||
| chr1:120176377-120176614 | Common:1; Rare:52 | ||||
| chr1:145823895-145824241 | Rare:122 | ||||
| chr1:145918695-145919013 | Common:2; Rare:64 | ||||
| chr1:145927393-145927644 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
| chr1:145964573-145964743 | Rare:43 | ||||
| chr1:147172427-147172730 | Common:1; Rare:81 | ||||
| chr1:148952190-148952402 | Common:1; Rare:58 | ||||
| chr1:149842745-149842919 | Rare:3 | ||||
| chr1:149850848-149851065 | Rare:1 | ||||
| chr1:149886668-149887004 | Common:1; Rare:117 | ||||
| chr1:149887829-149888215 | Rare:122 | ||||
| chr1:149927766-149927872 | Rare:42; Clinvar (benign):3 |