| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:178725123-178725312 | Common:10; Rare:74 | ||||
| chr1:179081912-179082086 | Common:1; Rare:54 | ||||
| chr1:179142992-179143255 | Common:1; Rare:55 | ||||
| chr1:179293614-179293933 | Common:3; Rare:100 | ||||
| chr1:179877739-179877898 | Rare:34 | ||||
| chr1:179882204-179882316 | Rare:21 | ||||
| chr1:179882368-179882724 | Rare:140; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:179882732-179882965 | Common:1; Rare:123; Clinvar:8; Clinvar (benign):2 | ||||
| chr1:179954691-179954814 | Rare:29 | ||||
| chr1:180155037-180155169 | Common:1; Rare:36 | ||||
| chr1:180502454-180502644 | Common:1; Rare:71 | ||||
| chr1:181022811-181022958 | Common:1; Rare:72 | ||||
| chr1:181088484-181088752 | Common:1; Rare:103 | ||||
| chr1:181088861-181089024 | Common:1; Rare:64 | ||||
| chr1:182391744-182392044 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):4 |