Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44820399-44820447 | Rare:16 | ||||
chr1:44987339-44987366 | Rare:3 | ||||
chr1:45190912-45191013 | Common:1; Rare:15 | ||||
chr1:45191247-45191364 | Common:1; Rare:25 | ||||
chr1:45303476-45303974 | Common:1; Rare:138 | ||||
chr1:45304010-45304285 | Rare:41 | ||||
chr1:45327835-45328073 | Rare:98 | ||||
chr1:45328323-45328428 | Common:1; Rare:25 | ||||
chr1:45328888-45328920 | Rare:7 | ||||
chr1:45328939-45329000 | Rare:13 | ||||
chr1:45329324-45329814 | Common:3; Rare:125; Clinvar:14; Clinvar (benign):15 | ||||
chr1:45335869-45336282 | Rare:66 | ||||
chr1:45403307-45403509 | Rare:32 | ||||
chr1:45490081-45490265 | Common:1; Rare:24 | ||||
chr1:45513502-45513817 | Common:3; Rare:66 |