Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44213341-44213501 | Common:1; Rare:29 | ||||
chr1:45339996-45340193 | Rare:65 | ||||
chr1:45500057-45500351 | Common:1; Rare:72; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521880-45522044 | Common:1; Rare:63 | ||||
chr1:45583931-45584051 | Rare:43 | ||||
chr1:45688049-45688243 | Common:1; Rare:54 | ||||
chr1:46198358-46198522 | Common:1; Rare:66; Clinvar:1 | ||||
chr1:46303128-46303248 | Common:1; Rare:28 | ||||
chr1:46303252-46303736 | Common:2; Rare:146 | ||||
chr1:47333773-47333928 | Rare:57 | ||||
chr1:50969998-50970254 | Rare:44 | ||||
chr1:52056123-52056353 | Common:1; Rare:66 | ||||
chr1:52404441-52404626 | Common:1; Rare:55 | ||||
chr1:53238470-53238611 | Common:2; Rare:57 | ||||
chr1:53946277-53946495 | Common:1; Rare:78 |