| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161766136-161766434 | Common:4; Rare:92 | ||||
| chr1:162023350-162023999 | Common:5; Rare:187; Clinvar (pathogenic):1 | ||||
| chr1:162497670-162497902 | Common:3; Rare:73 | ||||
| chr1:162561308-162561682 | Common:4; Rare:140 | ||||
| chr1:162630633-162630950 | Common:2; Rare:38 | ||||
| chr1:162631207-162631408 | Rare:40 | ||||
| chr1:162790516-162790781 | Common:4; Rare:76 | ||||
| chr1:162796956-162797292 | Common:3; Rare:47 | ||||
| chr1:163321723-163322057 | Common:1; Rare:91 | ||||
| chr1:165631116-165631293 | Common:4; Rare:56 | ||||
| chr1:165698478-165698633 | Common:2; Rare:89 | ||||
| chr1:165768719-165769019 | Common:2; Rare:116; Clinvar:1 | ||||
| chr1:166839322-166839553 | Rare:64 | ||||
| chr1:167630113-167630342 | Common:3; Rare:39 | ||||
| chr1:167935957-167936266 | Common:1; Rare:93 |