| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191014129-191014381 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677856-191678155 | Common:4; Rare:86 | ||||
| chr2:195657030-195657266 | Common:1; Rare:63 | ||||
| chr2:196171524-196171885 | Common:1; Rare:116 | ||||
| chr2:196176132-196176504 | Rare:60 | ||||
| chr2:196639480-196639758 | Rare:86 | ||||
| chr2:197310692-197311063 | Rare:81 | ||||
| chr2:197434995-197435243 | Rare:79 | ||||
| chr2:197453239-197453552 | Rare:104 | ||||
| chr2:197499780-197500006 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197500108-197500427 | Common:1; Rare:134 | ||||
| chr2:197515780-197516089 | Common:2; Rare:109 | ||||
| chr2:197705181-197705410 | Common:3; Rare:104 | ||||
| chr2:199911080-199911451 | Rare:127 | ||||
| chr2:200509907-200510239 | Common:2; Rare:114 |