| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49120755-49121150 | Rare:109; Clinvar:1 | ||||
| chr3:49121771-49121950 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:49132823-49133154 | Rare:77; Clinvar:3 | ||||
| chr3:49339976-49340110 | Common:2; Rare:67 | ||||
| chr3:49358141-49358469 | Common:4; Rare:166 | ||||
| chr3:49411827-49412445 | Common:2; Rare:215 | ||||
| chr3:49469922-49470349 | Common:2; Rare:138 | ||||
| chr3:49674225-49674402 | Common:1; Rare:70 | ||||
| chr3:49689451-49689599 | Rare:50 | ||||
| chr3:49786504-49786754 | Rare:82 | ||||
| chr3:50088834-50088991 | Rare:44 | ||||
| chr3:50299220-50299693 | Common:3; Rare:115 | ||||
| chr3:50328026-50328342 | Common:1; Rare:87 | ||||
| chr3:50350699-50350946 | Common:1; Rare:41 | ||||
| chr3:50350990-50351210 | Common:3; Rare:44 |