| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:213284210-213284483 | Rare:88 | ||||
| chr2:215311883-215312152 | Common:8; Rare:108 | ||||
| chr2:215435756-215435903 | Common:1; Rare:34 | ||||
| chr2:216081724-216081904 | Common:1; Rare:57 | ||||
| chr2:216412664-216412775 | Rare:13 | ||||
| chr2:216498680-216498894 | Common:7; Rare:86 | ||||
| chr2:216694533-216694767 | Rare:61 | ||||
| chr2:217905420-217905645 | Rare:44 | ||||
| chr2:217978797-217978947 | Common:1; Rare:44 | ||||
| chr2:218217058-218217246 | Common:1; Rare:67 | ||||
| chr2:218269985-218270565 | Common:6; Rare:186; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218271113-218271444 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218287258-218287406 | Rare:26 | ||||
| chr2:218289992-218290153 | Common:3; Rare:27 | ||||
| chr2:218292470-218292604 | Rare:35 |