| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197434970-197435186 | Rare:73 | ||||
| chr2:197453233-197453571 | Rare:114 | ||||
| chr2:197499773-197500439 | Common:2; Rare:253; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:197500636-197500732 | Rare:27 | ||||
| chr2:197515855-197516118 | Common:1; Rare:99 | ||||
| chr2:197705212-197705417 | Common:2; Rare:88; Clinvar:1 | ||||
| chr2:199850825-199851187 | Common:1; Rare:107 | ||||
| chr2:200305943-200306102 | Rare:28 | ||||
| chr2:200306433-200306582 | Common:2; Rare:35 | ||||
| chr2:200306606-200306907 | Common:2; Rare:98 | ||||
| chr2:200510026-200510201 | Rare:57 | ||||
| chr2:200526010-200526224 | Common:2; Rare:67 | ||||
| chr2:200811431-200811610 | Common:1; Rare:66 | ||||
| chr2:200864199-200864257 | Rare:21 | ||||
| chr2:200864580-200864788 | Common:1; Rare:78 |