| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:210476666-210476843 | Rare:58 | ||||
| chr2:210477560-210477690 | Rare:40 | ||||
| chr2:213284223-213284493 | Rare:88 | ||||
| chr2:215311879-215312128 | Common:7; Rare:95 | ||||
| chr2:215436032-215436234 | Common:2; Rare:68 | ||||
| chr2:216081756-216081939 | Common:1; Rare:64 | ||||
| chr2:216412705-216412781 | Rare:10 | ||||
| chr2:216498740-216498894 | Common:6; Rare:65 | ||||
| chr2:216694791-216695017 | Rare:39 | ||||
| chr2:216695536-216695846 | Rare:68 | ||||
| chr2:218216985-218217240 | Common:2; Rare:88 | ||||
| chr2:218270086-218270533 | Common:5; Rare:139; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218568301-218568640 | Common:3; Rare:92 | ||||
| chr2:218568733-218568946 | Common:1; Rare:59 | ||||
| chr2:218659621-218659738 | Rare:27 |