| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:183185944-183186297 | Common:4; Rare:74; Clinvar:3; Clinvar (benign):3 | ||||
| chr1:183472258-183472542 | Common:2; Rare:98 | ||||
| chr1:183635579-183636114 | Common:5; Rare:145 | ||||
| chr1:183636379-183636474 | Rare:12 | ||||
| chr1:184386673-184387368 | Common:4; Rare:175 | ||||
| chr1:185156699-185156800 | Common:1; Rare:42 | ||||
| chr1:185156923-185157300 | Common:1; Rare:103 | ||||
| chr1:185307517-185307863 | Common:1; Rare:72 | ||||
| chr1:185316963-185316980 | Rare:5 | ||||
| chr1:185317231-185317629 | Common:2; Rare:110 | ||||
| chr1:186375104-186375484 | Rare:111 | ||||
| chr1:186375636-186375919 | Common:1; Rare:80 | ||||
| chr1:190474460-190474681 | Common:2; Rare:36 | ||||
| chr1:190474763-190475175 | Common:2; Rare:90 | ||||
| chr1:190475805-190475944 | Common:2; Rare:30 |