| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190534697-190534870 | Common:1; Rare:56 | ||||
| chr2:190648709-190648916 | Common:1; Rare:75 | ||||
| chr2:191014133-191014512 | Common:3; Rare:113; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245288-191245570 | Common:2; Rare:90 | ||||
| chr2:191677858-191678173 | Common:4; Rare:90 | ||||
| chr2:191846820-191847581 | Rare:155 | ||||
| chr2:197434976-197435192 | Rare:73 | ||||
| chr2:197453242-197453561 | Rare:109 | ||||
| chr2:197499795-197500430 | Common:1; Rare:242; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500663-197500690 | Rare:7 | ||||
| chr2:200509907-200510134 | Common:1; Rare:83 | ||||
| chr2:200609068-200609372 | Rare:79 | ||||
| chr2:200811362-200811614 | Common:1; Rare:86 | ||||
| chr2:200864238-200864255 | Rare:5 | ||||
| chr2:200864551-200864806 | Common:1; Rare:92 |