| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71071650-71071855 | Common:1; Rare:90 | ||||
| chr2:71072107-71072392 | Common:1; Rare:47 | ||||
| chr2:71129912-71130079 | Common:1; Rare:29 | ||||
| chr2:71130087-71130426 | Common:3; Rare:117; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:71130435-71131109 | Common:6; Rare:176 | ||||
| chr2:71227056-71227419 | Common:2; Rare:88 | ||||
| chr2:71276440-71276620 | Rare:64 | ||||
| chr2:71331535-71331853 | Common:5; Rare:97 | ||||
| chr2:71331962-71332132 | Common:2; Rare:41 | ||||
| chr2:72887188-72887484 | Common:2; Rare:86; Clinvar (benign):1 | ||||
| chr2:72916013-72916430 | Common:1; Rare:126 | ||||
| chr2:72916439-72916659 | Rare:51 | ||||
| chr2:72917155-72917583 | Common:6; Rare:118 | ||||
| chr2:73070243-73070486 | Common:1; Rare:54 | ||||
| chr2:73071158-73071545 | Common:3; Rare:127 |