| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:211326646-211327001 | Common:7; Rare:103 | ||||
| chr1:211578951-211579474 | Rare:373 | ||||
| chr1:211675525-211675828 | Common:2; Rare:169 | ||||
| chr1:211829138-211830376 | Common:14; Rare:600 | ||||
| chr1:211830313-211830568 | Common:9; Rare:134 | ||||
| chr1:211830606-211830957 | Common:3; Rare:235 | ||||
| chr1:212035098-212035374 | Rare:74 | ||||
| chr1:212035461-212035831 | Common:7; Rare:283 | ||||
| chr1:212284969-212285663 | Common:16; Rare:509 | ||||
| chr1:212285728-212286009 | Common:3; Rare:180 | ||||
| chr1:212414727-212414998 | Common:6; Rare:168 | ||||
| chr1:212432725-212433029 | Rare:216 | ||||
| chr1:212608277-212608908 | Common:6; Rare:320 | ||||
| chr1:212791706-212792027 | Common:13; Rare:302 | ||||
| chr1:212858026-212858458 | Common:15; Rare:248; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):2 |