| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:15725035-15725336 | Common:4; Rare:87 | ||||
| chr1:15728465-15728726 | Common:2; Rare:49 | ||||
| chr1:15728884-15729122 | Common:1; Rare:62 | ||||
| chr1:15751788-15751971 | Common:1; Rare:47 | ||||
| chr1:15782517-15782652 | Common:1; Rare:13 | ||||
| chr1:15834920-15835133 | Common:1; Rare:91 | ||||
| chr1:15835785-15836117 | Common:6; Rare:154 | ||||
| chr1:16458640-16458872 | Common:1; Rare:53 | ||||
| chr1:16499217-16499367 | Rare:69 | ||||
| chr1:16644637-16644790 | Common:1; Rare:2 | ||||
| chr1:16913864-16914121 | Common:8; Rare:54 | ||||
| chr1:16955118-16955357 | Common:2; Rare:64 | ||||
| chr1:17619068-17619377 | Common:1; Rare:74 | ||||
| chr1:21827864-21828124 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:21857015-21857326 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):2 |