| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127885886-127885972 | Rare:19 | ||||
| chr2:128091055-128091351 | Common:8; Rare:98 | ||||
| chr2:130181546-130181700 | Common:1; Rare:54 | ||||
| chr2:130182089-130182353 | Common:2; Rare:104 | ||||
| chr2:130342111-130342265 | Rare:68; Clinvar:1 | ||||
| chr2:131492072-131492150 | Common:2; Rare:17 | ||||
| chr2:131492762-131493106 | Common:8; Rare:105 | ||||
| chr2:134918600-134918857 | Common:1; Rare:100 | ||||
| chr2:135052218-135052305 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr2:135531172-135531514 | Common:1; Rare:72 | ||||
| chr2:135985415-135985642 | Common:4; Rare:108; Clinvar (benign):1 | ||||
| chr2:138501681-138501931 | Common:1; Rare:89 | ||||
| chr2:148020681-148021011 | Common:2; Rare:71 | ||||
| chr2:149587690-149587877 | Common:1; Rare:53; Clinvar:1 | ||||
| chr2:151409788-151409954 | Common:2; Rare:47 |