| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3519370-3519586 | Common:2; Rare:73 | ||||
| chr2:3558251-3558478 | Common:5; Rare:101 | ||||
| chr2:3575107-3575447 | Common:2; Rare:98; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9003957-9004084 | Rare:54 | ||||
| chr2:9423098-9423677 | Common:2; Rare:149 | ||||
| chr2:9474500-9474575 | Common:6; Rare:45 | ||||
| chr2:9555615-9556052 | Common:2; Rare:145 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:9843179-9843544 | Common:7; Rare:114 | ||||
| chr2:10689924-10690024 | Common:2; Rare:33 | ||||
| chr2:11465867-11466181 | Common:3; Rare:93 | ||||
| chr2:11746389-11746657 | Common:2; Rare:73; Clinvar:3 | ||||
| chr2:12716753-12717048 | Common:1; Rare:87 | ||||
| chr2:17539719-17539980 | Common:2; Rare:50 | ||||
| chr2:17540532-17540802 | Common:2; Rare:62 |