| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219399987-219400111 | Rare:17 | ||||
| chr2:219418643-219418807 | Rare:60; Clinvar:14; Clinvar (benign):5 | ||||
| chr2:219498670-219498925 | Common:2; Rare:53 | ||||
| chr2:219543794-219544095 | Common:3; Rare:97 | ||||
| chr2:219552179-219552528 | Common:3; Rare:106; Clinvar (benign):1 | ||||
| chr2:219572046-219572492 | Common:2; Rare:109 | ||||
| chr2:219597737-219598258 | Common:3; Rare:189 | ||||
| chr2:219627119-219627219 | Rare:8 | ||||
| chr2:219627478-219627700 | Common:2; Rare:72 | ||||
| chr2:221572245-221572535 | Common:6; Rare:102 | ||||
| chr2:222656040-222656444 | Common:3; Rare:130 | ||||
| chr2:222860716-222861110 | Common:4; Rare:135 | ||||
| chr2:223945268-223945457 | Rare:83 | ||||
| chr2:223957293-223957482 | Common:3; Rare:73 | ||||
| chr2:224584691-224584897 | Rare:69 |