| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215311912-215312110 | Common:6; Rare:84 | ||||
| chr2:215364905-215365077 | Common:1; Rare:50 | ||||
| chr2:215375212-215375713 | Common:2; Rare:135 | ||||
| chr2:215409547-215410160 | Rare:168 | ||||
| chr2:215435656-215436166 | Common:3; Rare:126 | ||||
| chr2:216081777-216081932 | Common:1; Rare:54 | ||||
| chr2:216498732-216498887 | Common:5; Rare:65 | ||||
| chr2:216694470-216694658 | Rare:42 | ||||
| chr2:216694733-216694802 | Rare:18 | ||||
| chr2:218270091-218270568 | Common:5; Rare:151; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:218287258-218287398 | Rare:24 | ||||
| chr2:218292484-218292644 | Common:1; Rare:48 | ||||
| chr2:218322982-218323323 | Common:6; Rare:114 | ||||
| chr2:218381906-218382229 | Common:2; Rare:61 | ||||
| chr2:218568218-218568966 | Common:7; Rare:193 |