| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161314267-161314408 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr1:161505289-161505465 | Common:1; Rare:31 | ||||
| chr1:162497761-162497867 | Common:1; Rare:40 | ||||
| chr1:162790516-162790781 | Common:4; Rare:76 | ||||
| chr1:163321705-163321964 | Common:1; Rare:70 | ||||
| chr1:164559595-164559711 | Common:2; Rare:27 | ||||
| chr1:165768765-165769019 | Common:2; Rare:104 | ||||
| chr1:166839212-166839545 | Rare:97 | ||||
| chr1:167935957-167936327 | Common:2; Rare:112 | ||||
| chr1:167936561-167936711 | Rare:52 | ||||
| chr1:167936875-167936951 | Rare:29 | ||||
| chr1:168178878-168179083 | Common:1; Rare:77 | ||||
| chr1:168225901-168226056 | Common:1; Rare:55 | ||||
| chr1:169367764-169368254 | Common:3; Rare:93 | ||||
| chr1:169485705-169486197 | Common:1; Rare:144; Clinvar:6; Clinvar (benign):4 |