| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:100895796-100896159 | Common:1; Rare:99 | ||||
| chr1:101025725-101025951 | Common:1; Rare:65 | ||||
| chr1:101026077-101026215 | Rare:28 | ||||
| chr1:102879510-102879980 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:103525424-103525774 | Rare:99 | ||||
| chr1:103525890-103526194 | Common:1; Rare:94 | ||||
| chr1:107056570-107056869 | Common:1; Rare:131 | ||||
| chr1:108200116-108200654 | Common:11; Rare:146 | ||||
| chr1:108200890-108201170 | Common:2; Rare:71 | ||||
| chr1:108559891-108560108 | Common:1; Rare:73 | ||||
| chr1:108692168-108692402 | Common:2; Rare:87 | ||||
| chr1:108746435-108746768 | Common:3; Rare:119 | ||||
| chr1:108830593-108830790 | Common:1; Rare:68 | ||||
| chr1:108830950-108831170 | Common:1; Rare:28 | ||||
| chr1:108876794-108877057 | Common:2; Rare:73; Clinvar:4; Clinvar (benign):1 |