| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50256619-50256846 | Common:1; Rare:46 | ||||
| chr3:50278616-50278741 | Common:1; Rare:22 | ||||
| chr3:50292371-50292565 | Common:1; Rare:76 | ||||
| chr3:50299259-50299566 | Common:1; Rare:69 | ||||
| chr3:50321130-50321451 | Rare:91 | ||||
| chr3:50328137-50328353 | Common:1; Rare:64 | ||||
| chr3:50341400-50341596 | Common:1; Rare:57; Clinvar (benign):1 | ||||
| chr3:50345614-50345770 | Rare:29 | ||||
| chr3:50350511-50350663 | Rare:30 | ||||
| chr3:50350693-50350897 | Common:1; Rare:29 | ||||
| chr3:50359382-50359606 | Common:2; Rare:62 | ||||
| chr3:50365203-50365382 | Common:1; Rare:67 | ||||
| chr3:50567659-50567897 | Rare:78 | ||||
| chr3:50569421-50569504 | Rare:18 | ||||
| chr3:50611733-50611927 | Rare:43 |