| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215361967-215362329 | Common:1; Rare:98 | ||||
| chr2:215378174-215378465 | Common:1; Rare:64; Clinvar:1 | ||||
| chr2:215399058-215399216 | Common:1; Rare:26 | ||||
| chr2:215430715-215431045 | Rare:71; Clinvar (pathogenic):1 | ||||
| chr2:215433293-215433833 | Common:4; Rare:130 | ||||
| chr2:217795118-217795171 | Rare:9 | ||||
| chr2:217809057-217809371 | Common:22; Rare:55 | ||||
| chr2:217812118-217812464 | Common:3; Rare:74 | ||||
| chr2:217817376-217817927 | Common:5; Rare:139 | ||||
| chr2:217821808-217822062 | Common:1; Rare:69 | ||||
| chr2:217823410-217823769 | Common:2; Rare:61 | ||||
| chr2:217827317-217827518 | Rare:32 | ||||
| chr2:217830366-217830547 | Common:4; Rare:37 | ||||
| chr2:217831425-217831584 | Common:1; Rare:42 | ||||
| chr2:217840786-217840978 | Common:2; Rare:36 |