| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207805972-207806078 | Rare:14 | ||||
| chr2:207810840-207810973 | Common:2; Rare:24 | ||||
| chr2:207811051-207811293 | Rare:47 | ||||
| chr2:207930820-207930940 | Rare:31 | ||||
| chr2:208101843-208102137 | Common:3; Rare:54 | ||||
| chr2:208112980-208113370 | Common:6; Rare:79 | ||||
| chr2:208175360-208175660 | Common:4; Rare:63 | ||||
| chr2:208395349-208395502 | Rare:35 | ||||
| chr2:209340654-209340773 | Common:1; Rare:23 | ||||
| chr2:209368990-209369205 | Common:1; Rare:37 | ||||
| chr2:209639709-209640109 | Common:2; Rare:125 | ||||
| chr2:210195017-210195417 | Common:3; Rare:165; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210584974-210585119 | Rare:21 | ||||
| chr2:212940660-212941090 | Common:4; Rare:66 | ||||
| chr2:214019333-214019483 | Rare:50 |