Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91886235-91886326 | Rare:49 | ||||
chr1:92298945-92299089 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92831871-92832112 | Common:1; Rare:109; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92961430-92961581 | Rare:59 | ||||
chr1:93079123-93079299 | Common:2; Rare:72 | ||||
chr1:93179628-93179922 | Common:1; Rare:49 | ||||
chr1:93180360-93180712 | Common:1; Rare:153 | ||||
chr1:93345682-93345925 | Common:4; Rare:85 | ||||
chr1:93447980-93448147 | Common:2; Rare:60 | ||||
chr1:93909575-93909713 | Common:1; Rare:51 | ||||
chr1:94237529-94237758 | Rare:87 | ||||
chr1:94418096-94418470 | Common:3; Rare:135 | ||||
chr1:94541624-94541986 | Common:1; Rare:107 | ||||
chr1:94820190-94820401 | Common:3; Rare:57 | ||||
chr1:94903176-94903444 | Common:1; Rare:52 |