| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127107020-127107366 | Common:4; Rare:106; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:127294133-127294205 | Common:2; Rare:20; Clinvar (benign):2 | ||||
| chr2:127811150-127811229 | Rare:25 | ||||
| chr2:127885942-127885975 | Rare:4 | ||||
| chr2:130181538-130181704 | Common:2; Rare:60 | ||||
| chr2:130182091-130182561 | Common:3; Rare:176 | ||||
| chr2:130342621-130342938 | Common:6; Rare:108 | ||||
| chr2:130355754-130356085 | Common:4; Rare:95 | ||||
| chr2:130372569-130372782 | Common:1; Rare:60 | ||||
| chr2:131093369-131093593 | Common:1; Rare:103 | ||||
| chr2:131105245-131105372 | Common:1; Rare:64 | ||||
| chr2:131492089-131492266 | Common:3; Rare:62 | ||||
| chr2:131492279-131492567 | Common:8; Rare:116 | ||||
| chr2:131493026-131493097 | Common:1; Rare:20 | ||||
| chr2:134918597-134918917 | Common:1; Rare:136 |