| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3658080-3658238 | Common:3; Rare:30 | ||||
| chr2:3703457-3703754 | Common:11; Rare:86 | ||||
| chr2:9003957-9004097 | Rare:59 | ||||
| chr2:9423138-9424045 | Common:1; Rare:234 | ||||
| chr2:9474501-9474644 | Common:6; Rare:70 | ||||
| chr2:9555512-9556029 | Common:2; Rare:176; Clinvar:2 | ||||
| chr2:9630944-9631316 | Common:3; Rare:119 | ||||
| chr2:9843392-9843539 | Common:5; Rare:41 | ||||
| chr2:10043327-10043658 | Common:4; Rare:138; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:10044424-10044543 | Common:1; Rare:37 | ||||
| chr2:10368555-10368806 | Common:3; Rare:50 | ||||
| chr2:10689886-10690015 | Common:2; Rare:53 | ||||
| chr2:11344928-11345114 | Common:4; Rare:60 | ||||
| chr2:11465821-11466196 | Common:4; Rare:126 | ||||
| chr2:11482243-11482324 | Rare:16 |