| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885896-127885982 | Rare:23 | ||||
| chr2:128091031-128091338 | Common:8; Rare:103 | ||||
| chr2:130181546-130181709 | Common:1; Rare:62 | ||||
| chr2:130182091-130182330 | Common:2; Rare:93 | ||||
| chr2:130342127-130342281 | Rare:60 | ||||
| chr2:130342645-130342935 | Common:5; Rare:91 | ||||
| chr2:131093382-131093593 | Common:1; Rare:98 | ||||
| chr2:131493033-131493086 | Common:1; Rare:12 | ||||
| chr2:134918601-134918852 | Common:1; Rare:99 | ||||
| chr2:135531178-135531508 | Common:1; Rare:68 | ||||
| chr2:135985413-135985679 | Common:4; Rare:120; Clinvar (benign):1 | ||||
| chr2:137964100-137964494 | Common:2; Rare:61 | ||||
| chr2:144517308-144517739 | Common:5; Rare:133; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:148020688-148021103 | Common:2; Rare:95; Clinvar (benign):2 |