| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3519504-3519608 | Common:1; Rare:33 | ||||
| chr2:3558231-3558481 | Common:5; Rare:114 | ||||
| chr2:3575098-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9003957-9004084 | Rare:54 | ||||
| chr2:9423162-9423697 | Common:1; Rare:147 | ||||
| chr2:9474484-9474630 | Common:6; Rare:64 | ||||
| chr2:9555669-9555926 | Common:2; Rare:85 | ||||
| chr2:9630939-9631247 | Common:2; Rare:96 | ||||
| chr2:9843286-9843541 | Common:6; Rare:77 | ||||
| chr2:10689917-10690024 | Common:2; Rare:36 | ||||
| chr2:10812692-10812971 | Common:3; Rare:111 | ||||
| chr2:11466131-11466202 | Common:1; Rare:21 | ||||
| chr2:11746569-11746655 | Rare:31; Clinvar:2 | ||||
| chr2:12716748-12717053 | Common:1; Rare:88 | ||||
| chr2:12717689-12717923 | Rare:53 |