| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207769893-207770188 | Common:1; Rare:93 | ||||
| chr2:208254943-208255232 | Common:2; Rare:71 | ||||
| chr2:208266099-208266302 | Common:6; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002443-210002775 | Common:5; Rare:127 | ||||
| chr2:213284186-213284486 | Rare:96 | ||||
| chr2:215311852-215312142 | Common:8; Rare:109 | ||||
| chr2:215370292-215370593 | Common:10; Rare:94 | ||||
| chr2:215435794-215435903 | Rare:18 | ||||
| chr2:216081656-216081889 | Rare:79 | ||||
| chr2:216412705-216412775 | Rare:10 | ||||
| chr2:216498750-216498886 | Common:3; Rare:57 | ||||
| chr2:216694533-216694616 | Rare:16 | ||||
| chr2:216694633-216694767 | Rare:41 | ||||
| chr2:218217058-218217246 | Common:1; Rare:67 | ||||
| chr2:218269985-218270039 | Common:1; Rare:16 |