| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002257-176002394 | Common:1; Rare:52 | ||||
| chr2:177212566-177212791 | Common:2; Rare:98 | ||||
| chr2:177263449-177263651 | Common:1; Rare:45 | ||||
| chr2:177392659-177392845 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:183124252-183124407 | Common:4; Rare:50 | ||||
| chr2:186486024-186486344 | Common:3; Rare:88 | ||||
| chr2:189784319-189784543 | Common:3; Rare:81; Clinvar:7; Clinvar (benign):1 | ||||
| chr2:190534707-190535019 | Common:3; Rare:97 | ||||
| chr2:191014154-191014350 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:196799670-196799783 | Common:1; Rare:21 | ||||
| chr2:197499819-197500153 | Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500219-197500416 | Common:1; Rare:81 | ||||
| chr2:200889035-200889380 | Common:2; Rare:113 | ||||
| chr2:201071626-201071767 | Rare:30 | ||||
| chr2:201642653-201642736 | Rare:44 |