| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190648695-190649205 | Common:4; Rare:172 | ||||
| chr2:190880643-190880838 | Common:3; Rare:62 | ||||
| chr2:191014133-191014357 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245231-191245570 | Common:3; Rare:108 | ||||
| chr2:191246152-191246351 | Common:1; Rare:53 | ||||
| chr2:191677846-191678144 | Common:4; Rare:84 | ||||
| chr2:191678565-191678615 | Rare:24 | ||||
| chr2:192194913-192195077 | Rare:34 | ||||
| chr2:195656836-195657324 | Common:2; Rare:144 | ||||
| chr2:196593525-196593793 | Common:1; Rare:71 | ||||
| chr2:196639466-196639776 | Rare:101 | ||||
| chr2:196799585-196799787 | Common:1; Rare:66 | ||||
| chr2:197310727-197310984 | Rare:56 | ||||
| chr2:197434970-197435227 | Rare:83 | ||||
| chr2:197453101-197453563 | Rare:157 |