| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197705218-197705424 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:199911125-199911437 | Rare:109 | ||||
| chr2:200509867-200510210 | Common:1; Rare:125 | ||||
| chr2:200526016-200526207 | Common:2; Rare:57 | ||||
| chr2:200811288-200811592 | Common:1; Rare:94 | ||||
| chr2:200864229-200864255 | Rare:7 | ||||
| chr2:200864566-200864807 | Common:1; Rare:90 | ||||
| chr2:200888970-200889479 | Common:3; Rare:160 | ||||
| chr2:200963136-200963436 | Rare:67 | ||||
| chr2:200963536-200963915 | Common:1; Rare:104 | ||||
| chr2:201071543-201072052 | Rare:117 | ||||
| chr2:201115618-201116467 | Common:2; Rare:170 | ||||
| chr2:201116694-201117219 | Rare:95 | ||||
| chr2:201117399-201117601 | Rare:24 | ||||
| chr2:201118607-201118877 | Rare:41 |