Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20486198-20486369 | Rare:38 | ||||
chr1:20508041-20508216 | Common:2; Rare:62 | ||||
chr1:20661299-20661730 | Common:3; Rare:157; Clinvar:4; Clinvar (benign):7 | ||||
chr1:20787196-20787558 | Rare:166 | ||||
chr1:21176852-21177006 | Rare:45 | ||||
chr1:21345463-21345674 | Common:2; Rare:80 | ||||
chr1:21551063-21551333 | Common:1; Rare:51 | ||||
chr1:21782967-21783249 | Common:2; Rare:94 | ||||
chr1:21831010-21831247 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
chr1:22451644-22451878 | Common:1; Rare:73 | ||||
chr1:23368854-23368974 | Common:1; Rare:42 | ||||
chr1:23369797-23369959 | Rare:28 | ||||
chr1:23424623-23424897 | Common:1; Rare:80 | ||||
chr1:23558974-23559214 | Common:5; Rare:113 | ||||
chr1:23559335-23559643 | Common:1; Rare:134 |