| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219516937-219517337 | Common:1; Rare:115 | ||||
| chr2:219543736-219544087 | Common:3; Rare:106 | ||||
| chr2:219552300-219552590 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:219552646-219552781 | Rare:49 | ||||
| chr2:219570627-219571027 | Common:3; Rare:191; Clinvar:13; Clinvar (benign):7 | ||||
| chr2:219571406-219571641 | Common:1; Rare:58; Clinvar:3 | ||||
| chr2:219597087-219597491 | Rare:176 | ||||
| chr2:219597677-219597909 | Common:1; Rare:93 | ||||
| chr2:219598068-219598271 | Common:1; Rare:67 | ||||
| chr2:219627517-219627667 | Common:2; Rare:52 | ||||
| chr2:221569895-221570024 | Rare:23 | ||||
| chr2:221572263-221572596 | Common:6; Rare:118 | ||||
| chr2:221573569-221573836 | Rare:75 | ||||
| chr2:222656355-222656488 | Common:1; Rare:44 | ||||
| chr2:222860716-222861072 | Common:3; Rare:119 |