| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:21831217-21831527 | Common:1; Rare:96; Clinvar:3 | ||||
| chr1:21835538-21835822 | Common:2; Rare:64; Clinvar:1 | ||||
| chr1:21850147-21850475 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:21857014-21857325 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:21860176-21860414 | Rare:59; Clinvar:1 | ||||
| chr1:21872184-21872529 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:21876358-21876675 | Common:2; Rare:110; Clinvar:7; Clinvar (benign):2 | ||||
| chr1:21884765-21885168 | Common:1; Rare:125; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:21887215-21887682 | Common:3; Rare:178; Clinvar:13; Clinvar (benign):3 | ||||
| chr1:21907836-21908057 | Common:1; Rare:31 | ||||
| chr1:21926746-21927008 | Common:5; Rare:59 | ||||
| chr1:22509938-22510161 | Common:1; Rare:36 | ||||
| chr1:23068348-23068582 | Rare:48 | ||||
| chr1:23089015-23089196 | Common:2; Rare:45 | ||||
| chr1:23397540-23397970 | Common:1; Rare:128 |