| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218398096-218398233 | Common:1; Rare:44 | ||||
| chr2:218399517-218399791 | Common:1; Rare:123 | ||||
| chr2:218418993-218419133 | Rare:28 | ||||
| chr2:218568232-218568640 | Common:4; Rare:109 | ||||
| chr2:218568781-218568962 | Common:1; Rare:57 | ||||
| chr2:218659339-218659755 | Common:4; Rare:101 | ||||
| chr2:218671968-218672327 | Common:2; Rare:91 | ||||
| chr2:218748971-218749126 | Common:1; Rare:25 | ||||
| chr2:218782050-218782398 | Rare:111; Clinvar:14; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:219176897-219177114 | Common:4; Rare:65 | ||||
| chr2:219177819-219177917 | Common:3; Rare:19 | ||||
| chr2:219178142-219178466 | Common:6; Rare:134 | ||||
| chr2:219206687-219206946 | Rare:90 | ||||
| chr2:219229559-219229912 | Common:2; Rare:110 | ||||
| chr2:219245416-219245531 | Rare:33 |