Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16351980-16352191 | Common:2; Rare:52 | ||||
chr1:16352389-16352788 | Common:4; Rare:170 | ||||
chr1:16366959-16367346 | Common:1; Rare:122 | ||||
chr1:16367479-16367785 | Common:3; Rare:93 | ||||
chr1:16367858-16368040 | Common:3; Rare:38 | ||||
chr1:16440509-16440792 | Common:3; Rare:86 | ||||
chr1:16613277-16613379 | Common:1 | ||||
chr1:16613427-16613752 | Common:5; Rare:1 | ||||
chr1:16613864-16613977 | |||||
chr1:16980210-16980319 | Common:3; Rare:8 | ||||
chr1:16980567-16980721 | Rare:48 | ||||
chr1:17011895-17012145 | Common:2; Rare:68; Clinvar:1 | ||||
chr1:17053950-17054413 | Common:3; Rare:138; Clinvar:16; Clinvar (benign):12 | ||||
chr1:17119425-17119582 | Rare:39 | ||||
chr1:17437595-17438164 | Common:3; Rare:230 |