| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92831763-92832113 | Common:4; Rare:133; Clinvar:6; Clinvar (benign):5 | ||||
| chr1:92961430-92961809 | Common:3; Rare:114 | ||||
| chr1:93079067-93079329 | Common:4; Rare:112 | ||||
| chr1:93180092-93180762 | Common:2; Rare:262 | ||||
| chr1:93345774-93345919 | Common:4; Rare:57 | ||||
| chr1:93447976-93448217 | Common:2; Rare:84 | ||||
| chr1:93448219-93448367 | Common:1; Rare:39 | ||||
| chr1:93846627-93846765 | Common:1; Rare:46 | ||||
| chr1:93879144-93879308 | Common:3; Rare:58 | ||||
| chr1:94237536-94237731 | Rare:79 | ||||
| chr1:94418207-94418470 | Common:2; Rare:94 | ||||
| chr1:94541751-94541991 | Rare:70 | ||||
| chr1:94903141-94903444 | Common:1; Rare:60 | ||||
| chr1:94927047-94927350 | Common:1; Rare:105 | ||||
| chr1:95072866-95073032 | Common:2; Rare:64; Clinvar (benign):1 |