Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:165768768-165768933 | Common:1; Rare:72 | ||||
chr1:167935904-167936329 | Common:2; Rare:120 | ||||
chr1:167936553-167936919 | Common:1; Rare:130 | ||||
chr1:167936929-167936953 | Rare:7 | ||||
chr1:168225901-168226056 | Common:1; Rare:55 | ||||
chr1:169367750-169368276 | Common:3; Rare:105 | ||||
chr1:169485713-169486169 | Common:1; Rare:133; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794884-169795053 | Common:3; Rare:36 | ||||
chr1:170532038-170532192 | Rare:67; Clinvar:1 | ||||
chr1:170663031-170663354 | Common:1; Rare:70 | ||||
chr1:170664012-170664279 | Common:4; Rare:75 | ||||
chr1:171485404-171485602 | Rare:77 | ||||
chr1:171741918-171742151 | Common:1; Rare:74 | ||||
chr1:173477169-173477485 | Common:2; Rare:109 | ||||
chr1:173714782-173715057 | Common:2; Rare:62 |