| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191014123-191014333 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677858-191678147 | Common:4; Rare:81 | ||||
| chr2:192194907-192195077 | Rare:36 | ||||
| chr2:196926656-196926799 | Common:2; Rare:64 | ||||
| chr2:197434977-197435180 | Rare:67 | ||||
| chr2:197453227-197453554 | Rare:110 | ||||
| chr2:197499826-197500427 | Common:1; Rare:236; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515991-197516098 | Rare:46 | ||||
| chr2:197675688-197675856 | Rare:32 | ||||
| chr2:197705149-197705390 | Common:3; Rare:99 | ||||
| chr2:199455894-199456261 | Rare:81; Clinvar (benign):1 | ||||
| chr2:199457347-199457759 | Rare:76 | ||||
| chr2:200306429-200306586 | Common:2; Rare:36 | ||||
| chr2:200510040-200510263 | Common:1; Rare:69 | ||||
| chr2:200811431-200811572 | Common:1; Rare:50 |