| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219245393-219245531 | Rare:40 | ||||
| chr2:219253262-219253381 | Common:3; Rare:44 | ||||
| chr2:219253865-219254056 | Common:1; Rare:60 | ||||
| chr2:219498690-219498935 | Common:2; Rare:56 | ||||
| chr2:219552373-219552515 | Common:1; Rare:43 | ||||
| chr2:219597737-219597923 | Common:2; Rare:75 | ||||
| chr2:221501510-221501828 | Common:3; Rare:67 | ||||
| chr2:221572271-221572455 | Common:2; Rare:68 | ||||
| chr2:222298984-222299122 | Rare:27 | ||||
| chr2:222656027-222656460 | Common:3; Rare:144 | ||||
| chr2:223051308-223051375 | Common:1; Rare:16 | ||||
| chr2:223051615-223051824 | Common:3; Rare:56 | ||||
| chr2:223052086-223052226 | Rare:29 | ||||
| chr2:223837530-223837811 | Common:1; Rare:61 | ||||
| chr2:223957248-223957504 | Common:4; Rare:100; Clinvar (benign):1 |