| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50328158-50328386 | Rare:67 | ||||
| chr3:50337241-50337722 | Common:3; Rare:162 | ||||
| chr3:50350693-50350892 | Common:1; Rare:28 | ||||
| chr3:50359474-50359740 | Common:2; Rare:81 | ||||
| chr3:50365103-50365379 | Common:1; Rare:102; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:50503631-50503805 | Common:1; Rare:61 | ||||
| chr3:50569009-50569226 | Rare:43 | ||||
| chr3:50569385-50569530 | Rare:32 | ||||
| chr3:50611765-50611890 | Rare:28 | ||||
| chr3:50611973-50612344 | Common:1; Rare:86; Clinvar:1 | ||||
| chr3:50616800-50617220 | Common:8; Rare:76 | ||||
| chr3:50674710-50675080 | Common:2; Rare:102 | ||||
| chr3:51384951-51385345 | Common:2; Rare:119 | ||||
| chr3:51391041-51391307 | Common:1; Rare:67 | ||||
| chr3:51499945-51500391 | Common:1; Rare:98 |