Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44775447-44775599 | Rare:58 | ||||
chr1:44986516-44986747 | Common:2; Rare:45; Clinvar (benign):1 | ||||
chr1:45340000-45340237 | Rare:83; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45521836-45522087 | Common:1; Rare:99 | ||||
chr1:45686515-45686620 | Rare:35 | ||||
chr1:45687059-45687351 | Common:1; Rare:75 | ||||
chr1:45688028-45688216 | Common:1; Rare:43 | ||||
chr1:46198403-46198506 | Common:1; Rare:38; Clinvar:1 | ||||
chr1:46303225-46303769 | Common:2; Rare:169 | ||||
chr1:46340657-46340814 | Common:3; Rare:38 | ||||
chr1:46604233-46604443 | Rare:53 | ||||
chr1:47333773-47333984 | Common:2; Rare:72 | ||||
chr1:52055145-52055256 | Common:1; Rare:24 | ||||
chr1:52056163-52056350 | Rare:56 | ||||
chr1:52404441-52404618 | Common:1; Rare:53 |