| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:209675523-209675651 | Common:1; Rare:27 | ||||
| chr1:209806060-209806267 | Common:3; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:209827874-209828036 | Common:1; Rare:40 | ||||
| chr1:209937871-209938241 | Common:4; Rare:119 | ||||
| chr1:211259048-211259404 | Common:1; Rare:111 | ||||
| chr1:211675589-211675769 | Rare:35 | ||||
| chr1:212035529-212035748 | Common:1; Rare:54 | ||||
| chr1:212414811-212414963 | Common:3; Rare:46 | ||||
| chr1:212791746-212791940 | Common:4; Rare:87 | ||||
| chr1:212858076-212858303 | Common:4; Rare:59; Clinvar:2 | ||||
| chr1:213051006-213051371 | Common:1; Rare:103 | ||||
| chr1:214281016-214281264 | Common:2; Rare:106 | ||||
| chr1:214551575-214551876 | Common:2; Rare:106 | ||||
| chr1:214602949-214603250 | Common:1; Rare:82 | ||||
| chr1:217078248-217078457 | Common:1; Rare:28 |