| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201260429-201260588 | Rare:33 | ||||
| chr2:201451435-201451874 | Common:3; Rare:109 | ||||
| chr2:201642633-201642782 | Rare:70 | ||||
| chr2:201643401-201643561 | Common:1; Rare:48; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:201780868-201781243 | Common:3; Rare:114; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238610 | Rare:58; Clinvar:1 | ||||
| chr2:202265618-202265799 | Rare:64 | ||||
| chr2:202376415-202376545 | Rare:25; Clinvar:1 | ||||
| chr2:202377023-202377097 | Rare:23; Clinvar:1 | ||||
| chr2:202911580-202912571 | Common:5; Rare:252 | ||||
| chr2:203014665-203014948 | Common:1; Rare:87 | ||||
| chr2:203238908-203239050 | Common:1; Rare:56 | ||||
| chr2:203239196-203239319 | Rare:39 | ||||
| chr2:203328179-203328511 | Common:2; Rare:121 | ||||
| chr2:203328892-203328909 | Rare:3 |