| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:102879642-102879848 | Rare:53; Clinvar (benign):2 | ||||
| chr1:103525442-103525784 | Rare:95 | ||||
| chr1:103525847-103526247 | Common:1; Rare:122 | ||||
| chr1:103526328-103526361 | Common:1; Rare:4 | ||||
| chr1:103526373-103526466 | Rare:16 | ||||
| chr1:107056538-107056887 | Common:2; Rare:149 | ||||
| chr1:107056928-107056969 | Rare:13 | ||||
| chr1:107139819-107140288 | Common:1; Rare:127 | ||||
| chr1:107140315-107140410 | Rare:18 | ||||
| chr1:107140466-107140546 | Rare:17 | ||||
| chr1:107140642-107140705 | Rare:10 | ||||
| chr1:107140813-107141049 | Rare:49 | ||||
| chr1:107141119-107141247 | Common:1; Rare:32 | ||||
| chr1:107141374-107141466 | Rare:35 | ||||
| chr1:107141474-107141692 | Common:1; Rare:76 |