| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:48301332-48301648 | Common:4; Rare:102 | ||||
| chr3:48440035-48440323 | Common:1; Rare:109 | ||||
| chr3:48473019-48473172 | Common:1; Rare:32 | ||||
| chr3:48504048-48504277 | Common:2; Rare:74 | ||||
| chr3:48556780-48557173 | Common:1; Rare:89 | ||||
| chr3:48918702-48918933 | Common:2; Rare:121 | ||||
| chr3:48989728-48989885 | Rare:40 | ||||
| chr3:49007111-49007429 | Common:2; Rare:129 | ||||
| chr3:49021502-49021721 | Rare:55; Clinvar:1 | ||||
| chr3:49029355-49029564 | Common:2; Rare:152 | ||||
| chr3:49104729-49104928 | Rare:82; Clinvar (benign):3 | ||||
| chr3:49120767-49120956 | Rare:60 | ||||
| chr3:49121745-49121984 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:49132969-49133143 | Rare:37; Clinvar:2 | ||||
| chr3:49276851-49277163 | Common:2; Rare:127 |