| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127526429-127526588 | Common:2; Rare:51 | ||||
| chr2:127811139-127811264 | Rare:37 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885892-127886531 | Common:2; Rare:177 | ||||
| chr2:128091031-128091335 | Common:8; Rare:102 | ||||
| chr2:130181546-130181801 | Common:3; Rare:114 | ||||
| chr2:130182087-130182381 | Common:2; Rare:113 | ||||
| chr2:130342069-130342242 | Rare:71; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:130342282-130342313 | Rare:11 | ||||
| chr2:130342639-130342935 | Common:5; Rare:93 | ||||
| chr2:130756109-130756360 | Common:2; Rare:86 | ||||
| chr2:131093343-131093555 | Common:1; Rare:95 | ||||
| chr2:131105214-131105375 | Common:1; Rare:74 | ||||
| chr2:131492754-131493118 | Common:8; Rare:111 | ||||
| chr2:134918580-134918863 | Common:1; Rare:111 |