Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173867969-173868380 | Common:2; Rare:140 | ||||
chr1:174022356-174022483 | Rare:32 | ||||
chr1:174799432-174799776 | Rare:60 | ||||
chr1:174999620-175000088 | Common:1; Rare:137 | ||||
chr1:179882158-179882341 | Common:1; Rare:36 | ||||
chr1:179882488-179882943 | Common:1; Rare:225; Clinvar:9; Clinvar (benign):4 | ||||
chr1:180940854-180941050 | Common:7; Rare:54 | ||||
chr1:182391316-182391432 | Rare:23 | ||||
chr1:182789475-182789778 | Common:4; Rare:90 | ||||
chr1:182839048-182839367 | Common:1; Rare:103 | ||||
chr1:183472234-183472538 | Common:2; Rare:102 | ||||
chr1:183635634-183636097 | Common:4; Rare:131 | ||||
chr1:184386886-184387172 | Rare:75 | ||||
chr1:185156710-185156789 | Common:1; Rare:33 | ||||
chr1:185156934-185157313 | Common:1; Rare:102 |