| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203238864-203239026 | Rare:61 | ||||
| chr2:203328018-203328461 | Common:2; Rare:153 | ||||
| chr2:205682356-205682563 | Rare:35 | ||||
| chr2:206085824-206085963 | Common:1; Rare:38 | ||||
| chr2:206159347-206159982 | Common:4; Rare:185; Clinvar (benign):1 | ||||
| chr2:206274916-206275041 | Rare:47 | ||||
| chr2:206765284-206765616 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:207529662-207530025 | Common:3; Rare:112 | ||||
| chr2:207625262-207625498 | Common:1; Rare:71 | ||||
| chr2:207711331-207711526 | Common:1; Rare:59 | ||||
| chr2:208025496-208025618 | Rare:32 | ||||
| chr2:208255032-208255234 | Common:2; Rare:52 | ||||
| chr2:208266070-208266401 | Common:7; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423788-209424120 | Common:1; Rare:101 | ||||
| chr2:210002461-210002659 | Common:5; Rare:62 |