Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:31741937-31742080 | Common:2; Rare:39 | ||||
chr1:36703808-36703925 | Common:1; Rare:23 | ||||
chr1:39559330-39559396 | Rare:12 | ||||
chr1:42924271-42924460 | Common:1; Rare:59 | ||||
chr1:42929732-42929965 | Common:2; Rare:58; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):5 | ||||
chr1:43990185-43990456 | Common:1; Rare:83 | ||||
chr1:44048258-44048464 | Common:1; Rare:24 | ||||
chr1:44731162-44731295 | Common:4; Rare:54 | ||||
chr1:46442611-46442888 | Common:1; Rare:52 | ||||
chr1:46489666-46489936 | Common:4; Rare:70 | ||||
chr1:51423454-51423547 | Common:1; Rare:18 | ||||
chr1:60867936-60868026 | Rare:20 | ||||
chr1:60970668-60970700 | Rare:8 | ||||
chr1:61056832-61057035 | Common:2; Rare:50 | ||||
chr1:61230720-61230739 | Rare:2 |