| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196593518-196593749 | Common:1; Rare:61 | ||||
| chr2:196639466-196639783 | Rare:102 | ||||
| chr2:196713012-196713159 | Common:1; Rare:41 | ||||
| chr2:196799562-196799798 | Common:2; Rare:79 | ||||
| chr2:196926722-196926855 | Common:2; Rare:48 | ||||
| chr2:197311169-197311322 | Rare:27 | ||||
| chr2:197434939-197435192 | Rare:86 | ||||
| chr2:197453233-197453571 | Rare:114 | ||||
| chr2:197499807-197500441 | Common:1; Rare:244; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515808-197516127 | Common:2; Rare:114 | ||||
| chr2:197675571-197675774 | Common:10; Rare:42 | ||||
| chr2:197705212-197705390 | Common:2; Rare:66 | ||||
| chr2:197785069-197785415 | Common:5; Rare:87 | ||||
| chr2:199911005-199911582 | Common:2; Rare:206 | ||||
| chr2:200306257-200306562 | Common:5; Rare:76 |