| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16904815-16904978 | Common:2; Rare:19 | ||||
| chr1:16913846-16914115 | Common:8; Rare:53 | ||||
| chr1:18111085-18111132 | Common:2; Rare:17 | ||||
| chr1:19198546-19198825 | Common:2; Rare:67 | ||||
| chr1:20644229-20644540 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:20650390-20650491 | Common:1; Rare:34 | ||||
| chr1:20655484-20655586 | Rare:36; Clinvar (benign):1 | ||||
| chr1:21293030-21293342 | Common:2; Rare:52 | ||||
| chr1:21827870-21828196 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:21831462-21831671 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:21831766-21831950 | Common:1; Rare:46; Clinvar:1 | ||||
| chr1:21857014-21857324 | Common:1; Rare:95; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:21861754-21862009 | Rare:80; Clinvar:6; Clinvar (benign):1 | ||||
| chr1:21884777-21885131 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:22025183-22025532 | Common:7; Rare:89 |