| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69829508-69829741 | Common:1; Rare:95 | ||||
| chr2:70086890-70087118 | Common:1; Rare:114 | ||||
| chr2:70087307-70088034 | Common:2; Rare:244 | ||||
| chr2:70258007-70258242 | Common:2; Rare:85 | ||||
| chr2:70293631-70293841 | Common:2; Rare:69 | ||||
| chr2:70978503-70978647 | Rare:40 | ||||
| chr2:71068526-71068699 | Rare:80 | ||||
| chr2:71130194-71130677 | Common:6; Rare:140; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73071663-73071863 | Common:3; Rare:82 | ||||
| chr2:73112898-73113153 | Common:2; Rare:72 | ||||
| chr2:73214172-73214339 | Common:1; Rare:70 | ||||
| chr2:73233168-73233504 | Common:2; Rare:101 | ||||
| chr2:73233951-73234381 | Common:4; Rare:102 | ||||
| chr2:73385644-73386090 | Common:4; Rare:211; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73828804-73829024 | Common:1; Rare:51 |