| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:196926705-196926881 | Common:3; Rare:66 | ||||
| chr2:197434971-197435192 | Rare:75 | ||||
| chr2:197453227-197453563 | Rare:116 | ||||
| chr2:197499788-197500439 | Common:2; Rare:248; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:197515780-197516098 | Common:2; Rare:111 | ||||
| chr2:197675567-197675826 | Common:10; Rare:54 | ||||
| chr2:200306420-200306566 | Common:2; Rare:34 | ||||
| chr2:200509913-200510113 | Common:1; Rare:75 | ||||
| chr2:200526034-200526171 | Common:1; Rare:34 | ||||
| chr2:200585851-200586116 | Rare:68 | ||||
| chr2:200811432-200811580 | Common:1; Rare:52 | ||||
| chr2:200864542-200864763 | Common:1; Rare:73 | ||||
| chr2:200888989-200889441 | Common:3; Rare:143 | ||||
| chr2:200963581-200963871 | Common:1; Rare:77 | ||||
| chr2:201071592-201072047 | Rare:99 |