| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068539-71068686 | Rare:63 | ||||
| chr2:71130220-71130677 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:72825801-72826090 | Rare:92 | ||||
| chr2:73071298-73071522 | Common:1; Rare:77 | ||||
| chr2:73071694-73071863 | Common:2; Rare:65 | ||||
| chr2:73234276-73234368 | Common:1; Rare:40 | ||||
| chr2:73385729-73386121 | Common:4; Rare:201; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr2:73737304-73737485 | Common:2; Rare:56 | ||||
| chr2:73828804-73829020 | Common:1; Rare:50 | ||||
| chr2:74147870-74148111 | Common:1; Rare:64; Clinvar:2 | ||||
| chr2:74440551-74440650 | Rare:26 | ||||
| chr2:74454813-74455130 | Rare:83 | ||||
| chr2:74455522-74455882 | Rare:82 | ||||
| chr2:74458146-74458498 | Common:1; Rare:106 | ||||
| chr2:74459683-74460028 | Rare:125 |