| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11664043-11664489 | Common:2; Rare:120 | ||||
| chr1:11664549-11664829 | Common:2; Rare:69 | ||||
| chr1:11664869-11665027 | Common:2; Rare:37 | ||||
| chr1:11681072-11681310 | Common:2; Rare:83 | ||||
| chr1:11735965-11736202 | Common:3; Rare:70 | ||||
| chr1:11736411-11736649 | Common:1; Rare:57 | ||||
| chr1:11772571-11772641 | Common:1; Rare:12 | ||||
| chr1:11802769-11802808 | Rare:12 | ||||
| chr1:11803118-11803296 | Common:1; Rare:43; Clinvar (pathogenic):1 | ||||
| chr1:11803511-11803738 | Rare:52 | ||||
| chr1:11804871-11805047 | Common:1; Rare:29 | ||||
| chr1:11805445-11805588 | Common:1; Rare:24 | ||||
| chr1:11805857-11806295 | Common:2; Rare:125; Clinvar:2 | ||||
| chr1:11806423-11806511 | Rare:17 | ||||
| chr1:11926380-11926644 | Common:6; Rare:72 |