Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367770-169368263 | Common:3; Rare:94 | ||||
chr1:169794889-169795079 | Common:3; Rare:45 | ||||
chr1:170532006-170532178 | Common:1; Rare:67; Clinvar:1 | ||||
chr1:170663255-170663599 | Common:2; Rare:62 | ||||
chr1:170663787-170664167 | Common:4; Rare:75 | ||||
chr1:173477141-173477491 | Common:4; Rare:128 | ||||
chr1:173714874-173714975 | Rare:25 | ||||
chr1:173824405-173824714 | Rare:57; Clinvar:2 | ||||
chr1:179081889-179082098 | Common:1; Rare:64 | ||||
chr1:179882488-179882852 | Rare:173; Clinvar:7; Clinvar (benign):2 | ||||
chr1:180154638-180154904 | Common:3; Rare:84 | ||||
chr1:182789639-182789778 | Common:2; Rare:45 | ||||
chr1:182839034-182839355 | Common:2; Rare:99 | ||||
chr1:183635609-183636094 | Common:4; Rare:135 | ||||
chr1:184386736-184387172 | Common:3; Rare:124 |