| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:31644852-31645002 | Not yet | Common:3; Rare:48 | 111 | ||
| chr1:32292035-32292215 | Not yet | Rare:67 | 80 | ||
| chr1:32650929-32651226 | Not yet | Common:2; Rare:99 | 147 | ||
| chr1:32817294-32817679 | Not yet | Rare:96; Clinvar:5 | 158 | ||
| chr1:34985303-34985389 | Not yet | Common:1; Rare:27 | 69 | ||
| chr1:35181742-35181875 | Not yet | Rare:29 | 81 | ||
| chr1:35193108-35193159 | Not yet | Rare:28 | 49 | ||
| chr1:35557373-35557465 | Not yet | Rare:18 | 69 | ||
| chr1:35557597-35557834 | Not yet | Common:2; Rare:86 | 107 | ||
| chr1:35641459-35641629 | Not yet | Rare:37 | 117 | ||
| chr1:36149420-36149822 | Not yet | Common:3; Rare:111 | 174 | ||
| chr1:36155847-36156163 | Not yet | Rare:118 | 122 | ||
| chr1:36464236-36464490 | Not yet | Common:2; Rare:75 | 150 | ||
| chr1:36467556-36467851 | Not yet | Common:1; Rare:76; Clinvar:2; Clinvar (benign):1 | 135 | ||
| chr1:36472242-36472678 | Not yet | Common:4; Rare:140; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | 141 |