Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:204411375-204411435 | Rare:23; Clinvar:1 | ||||
chr1:204411761-204412293 | Common:13; Rare:152 | ||||
chr1:204493779-204494233 | Rare:93 | ||||
chr1:204494350-204494403 | Rare:7 | ||||
chr1:204494633-204494956 | Common:1; Rare:102 | ||||
chr1:204516047-204516097 | Rare:8 | ||||
chr1:204516127-204516853 | Common:2; Rare:183 | ||||
chr1:205121882-205122496 | Common:5; Rare:173 | ||||
chr1:205211153-205211408 | Common:1; Rare:86 | ||||
chr1:205211443-205211629 | Common:1; Rare:87; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:205211647-205211753 | Rare:24 | ||||
chr1:205227738-205227989 | Common:1; Rare:81 | ||||
chr1:205321708-205321988 | Common:2; Rare:82 | ||||
chr1:205449942-205450204 | Common:3; Rare:80 | ||||
chr1:205504394-205504747 | Common:5; Rare:65 |