| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:116373090-116373349 | Rare:88 | ||||
| chr1:116570970-116571167 | Common:2; Rare:60 | ||||
| chr1:117060060-117060374 | Common:6; Rare:90 | ||||
| chr1:117121726-117121957 | Common:1; Rare:63 | ||||
| chr1:117929547-117929861 | Common:4; Rare:95 | ||||
| chr1:119140616-119140782 | Common:1; Rare:58 | ||||
| chr1:120069594-120069796 | Common:4; Rare:52 | ||||
| chr1:120176310-120176621 | Common:1; Rare:62 | ||||
| chr1:144461580-144461697 | Common:4; Rare:53 | ||||
| chr1:145607851-145608093 | Common:2; Rare:75 | ||||
| chr1:145823848-145824009 | Rare:54 | ||||
| chr1:145824012-145824274 | Rare:95 | ||||
| chr1:145858996-145859173 | Rare:51 | ||||
| chr1:145918658-145919022 | Common:2; Rare:91; Clinvar:1 | ||||
| chr1:145927193-145927358 | Common:1; Rare:39; Clinvar (benign):1; Clinvar (pathogenic):1 |