| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:54801165-54801442 | Common:2; Rare:61 | ||||
| chr1:54801526-54801644 | Common:1; Rare:26 | ||||
| chr1:54886564-54886923 | Common:1; Rare:132 | ||||
| chr1:54887096-54887469 | Common:3; Rare:122; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:54887501-54887655 | Rare:26 | ||||
| chr1:54980559-54980701 | Common:3; Rare:27 | ||||
| chr1:55214611-55214986 | Common:2; Rare:108 | ||||
| chr1:55215076-55215166 | Rare:26 | ||||
| chr1:55215208-55215965 | Common:3; Rare:244 | ||||
| chr1:56516988-56517135 | Common:1; Rare:21 | ||||
| chr1:56579222-56579514 | Common:3; Rare:65 | ||||
| chr1:56579641-56579861 | Common:2; Rare:26 | ||||
| chr1:56645127-56645179 | Rare:12 | ||||
| chr1:56645198-56645422 | Common:1; Rare:75 | ||||
| chr1:58546169-58546451 | Common:4; Rare:60 |