| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200864618-200864821 | Rare:78 | ||||
| chr2:200888989-200889471 | Common:3; Rare:151 | ||||
| chr2:200963555-200963897 | Common:1; Rare:93 | ||||
| chr2:201071615-201072050 | Rare:91 | ||||
| chr2:201451450-201451826 | Common:2; Rare:96 | ||||
| chr2:201642622-201642775 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr2:201643435-201643493 | Rare:21; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:202238443-202238664 | Rare:79; Clinvar:1 | ||||
| chr2:202265536-202265791 | Common:1; Rare:76 | ||||
| chr2:202911857-202912038 | Rare:38 | ||||
| chr2:202912119-202912541 | Common:4; Rare:124 | ||||
| chr2:203238827-203239068 | Common:2; Rare:99 | ||||
| chr2:203328028-203328555 | Common:2; Rare:178 | ||||
| chr2:203535246-203535546 | Common:3; Rare:131 | ||||
| chr2:206085771-206085960 | Common:1; Rare:54 |