| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218408279-218408404 | Rare:18 | ||||
| chr2:218569908-218570105 | Common:1; Rare:41 | ||||
| chr2:218631936-218632186 | Rare:42 | ||||
| chr2:218759288-218759682 | Common:1; Rare:67 | ||||
| chr2:218782737-218783018 | Common:2; Rare:33 | ||||
| chr2:218809470-218809684 | Rare:58; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:219069534-219069554 | Rare:2 | ||||
| chr2:219211646-219211925 | Common:1; Rare:36 | ||||
| chr2:219237329-219237399 | Rare:22 | ||||
| chr2:221440883-221441163 | Common:1; Rare:53 | ||||
| chr2:221453374-221453664 | Common:4; Rare:55 | ||||
| chr2:221467756-221467927 | Rare:25 | ||||
| chr2:221516305-221516342 | Rare:8 | ||||
| chr2:221780547-221780556 | Rare:1 | ||||
| chr2:222645163-222645460 | Common:1; Rare:46 |