| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3379490-3379961 | Common:17; Rare:608 | ||||
| chr2:3380032-3380432 | Common:6; Rare:149 | ||||
| chr2:3518780-3519310 | Common:12; Rare:604 | ||||
| chr2:3519333-3519733 | Common:17; Rare:467 | ||||
| chr2:3558180-3558753 | Common:41; Rare:1140 | ||||
| chr2:3558714-3559114 | Common:7; Rare:73 | ||||
| chr2:3574920-3575430 | Common:15; Rare:645; Clinvar:21; Clinvar (benign):41 | ||||
| chr2:3575652-3576052 | Common:5; Rare:183; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:3594770-3595350 | Common:2; Rare:298 | ||||
| chr2:3601547-3601983 | Common:14; Rare:206 | ||||
| chr2:3604376-3605707 | Common:29; Rare:532 | ||||
| chr2:6864940-6865610 | Rare:526 | ||||
| chr2:6865630-6866010 | Common:12; Rare:389 | ||||
| chr2:6866030-6866500 | Common:6; Rare:240 | ||||
| chr2:6877530-6877790 | Common:4; Rare:45 |