Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:48446640-48446743 | Rare:37 | ||||
chr3:48504084-48504281 | Common:2; Rare:61 | ||||
chr3:48556740-48557173 | Common:1; Rare:105 | ||||
chr3:48635407-48635659 | Common:1; Rare:81 | ||||
chr3:48847781-48847957 | Rare:62 | ||||
chr3:48918707-48918895 | Common:2; Rare:95 | ||||
chr3:49007181-49007424 | Common:2; Rare:94 | ||||
chr3:49021503-49021725 | Rare:55; Clinvar:1 | ||||
chr3:49029355-49029564 | Common:2; Rare:152 | ||||
chr3:49104729-49104919 | Rare:79; Clinvar (benign):3 | ||||
chr3:49132979-49133124 | Rare:33; Clinvar:1 | ||||
chr3:49199290-49199536 | Common:1; Rare:57 | ||||
chr3:49277058-49277129 | Rare:25 | ||||
chr3:49340020-49340270 | Common:3; Rare:83 | ||||
chr3:49358237-49358522 | Common:4; Rare:143 |