Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39956321-39956541 | Common:3; Rare:40 | ||||
chr1:39956647-39957271 | Rare:130 | ||||
chr1:39969369-39969649 | Common:1; Rare:74 | ||||
chr1:42929596-42930018 | Common:2; Rare:107; Clinvar:8; Clinvar (benign):16; Clinvar (pathogenic):6 | ||||
chr1:42955936-42956113 | Rare:34 | ||||
chr1:43119927-43120158 | Common:7; Rare:72 | ||||
chr1:43445996-43446186 | Rare:57 | ||||
chr1:43609461-43609663 | Common:1; Rare:49 | ||||
chr1:44001027-44001176 | Common:1; Rare:36 | ||||
chr1:44001216-44001445 | Common:2; Rare:64 | ||||
chr1:44029983-44030131 | Rare:56 | ||||
chr1:44216479-44216796 | Common:2; Rare:63 | ||||
chr1:44776278-44776492 | Rare:44 | ||||
chr1:46718204-46718541 | Common:2; Rare:68 | ||||
chr1:51257735-51257948 | Common:3; Rare:34 |