| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121755415-121755761 | Common:4; Rare:115 | ||||
| chr2:127294100-127294227 | Common:2; Rare:51; Clinvar (benign):2 | ||||
| chr2:127387973-127388255 | Common:7; Rare:124 | ||||
| chr2:127526422-127526619 | Common:2; Rare:66 | ||||
| chr2:127811139-127811224 | Rare:28 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885886-127885995 | Rare:29 | ||||
| chr2:128091031-128091370 | Common:8; Rare:109 | ||||
| chr2:130181546-130181696 | Common:1; Rare:53 | ||||
| chr2:130182089-130182347 | Common:2; Rare:101 | ||||
| chr2:130342118-130342279 | Rare:66; Clinvar:1 | ||||
| chr2:130342645-130342935 | Common:5; Rare:91 | ||||
| chr2:131105214-131105356 | Common:1; Rare:60 | ||||
| chr2:131493040-131493097 | Common:1; Rare:15 | ||||
| chr2:134918589-134918870 | Common:1; Rare:114 |