| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219461271-219461431 | Rare:34 | ||||
| chr2:219498514-219498944 | Common:2; Rare:92 | ||||
| chr2:219571494-219571734 | Rare:46 | ||||
| chr2:219571952-219572308 | Common:12; Rare:82 | ||||
| chr2:219597737-219597909 | Common:1; Rare:70 | ||||
| chr2:221572271-221572535 | Common:6; Rare:95 | ||||
| chr2:222298701-222298779 | Rare:22; Clinvar:1 | ||||
| chr2:223957256-223957475 | Common:4; Rare:81 | ||||
| chr2:226835895-226836130 | Common:1; Rare:94 | ||||
| chr2:227325148-227325480 | Common:6; Rare:122 | ||||
| chr2:227325755-227326069 | Rare:72 | ||||
| chr2:227718020-227718118 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr2:228181611-228181828 | Rare:67 | ||||
| chr2:229921899-229922522 | Common:4; Rare:220 | ||||
| chr2:229923159-229923404 | Common:1; Rare:58 |