| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:10474847-10474984 | Rare:43; Clinvar:1 | ||||
| chr1:11012261-11012379 | Rare:29 | ||||
| chr1:11099748-11099935 | Common:3; Rare:77 | ||||
| chr1:11262478-11262876 | Common:3; Rare:120 | ||||
| chr1:11654769-11654918 | Common:2; Rare:45 | ||||
| chr1:11805935-11806265 | Common:2; Rare:89; Clinvar:1 | ||||
| chr1:11934480-11934758 | Common:5; Rare:91; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:11980051-11980484 | Common:6; Rare:134; Clinvar:1; Clinvar (benign):5 | ||||
| chr1:12019284-12019545 | Common:5; Rare:95 | ||||
| chr1:12229920-12230099 | Common:1; Rare:53 | ||||
| chr1:13749129-13749451 | Common:2; Rare:111 | ||||
| chr1:14598380-14598691 | Common:1; Rare:93 | ||||
| chr1:15152440-15152615 | Rare:27 | ||||
| chr1:15153591-15153728 | Common:1; Rare:35 | ||||
| chr1:15526539-15526905 | Common:2; Rare:119 |