| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:94237356-94237744 | Rare:136 | ||||
| chr1:94418128-94418492 | Common:2; Rare:129 | ||||
| chr1:94541749-94541974 | Rare:70 | ||||
| chr1:94901531-94901785 | Common:2; Rare:57 | ||||
| chr1:94903012-94903099 | Common:1; Rare:16 | ||||
| chr1:94903119-94903546 | Common:1; Rare:85 | ||||
| chr1:94925589-94926033 | Common:2; Rare:96 | ||||
| chr1:94926844-94927498 | Common:4; Rare:207 | ||||
| chr1:95072817-95073008 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr1:95233971-95234266 | Common:5; Rare:97 | ||||
| chr1:96721648-96721867 | Common:1; Rare:97 | ||||
| chr1:97920887-97921070 | Rare:64; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr1:98661249-98661349 | Common:2; Rare:17 | ||||
| chr1:98661596-98661908 | Common:2; Rare:107 | ||||
| chr1:99645281-99645607 | Common:1; Rare:63 |