| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:59147250-59147490 | Rare:46 | ||||
| chr1:59272501-59272911 | Common:5; Rare:152 | ||||
| chr1:59354610-59355100 | Common:5; Rare:177 | ||||
| chr1:59355330-59355690 | Common:4; Rare:59 | ||||
| chr1:59378227-59378365 | Common:1; Rare:25 | ||||
| chr1:59409580-59410000 | Common:11; Rare:79 | ||||
| chr1:59432397-59433120 | Common:14; Rare:319 | ||||
| chr1:59515541-59515730 | Rare:41 | ||||
| chr1:59605165-59605383 | Rare:35 | ||||
| chr1:61077960-61078230 | Rare:44 | ||||
| chr1:62122254-62122654 | Common:2; Rare:152 | ||||
| chr1:62613205-62613605 | Rare:114 | ||||
| chr1:62625410-62625818 | Common:1; Rare:152; Clinvar (benign):1 | ||||
| chr1:62687307-62687470 | Rare:33 | ||||
| chr1:62725219-62725619 | Rare:75 |