Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:71069209-71069332 | Rare:31 | ||||
chr1:71080937-71081376 | Rare:114 | ||||
chr1:72282690-72283033 | Common:5; Rare:117 | ||||
chr1:74198126-74198351 | Common:3; Rare:120 | ||||
chr1:74732980-74733334 | Common:6; Rare:124 | ||||
chr1:74733374-74733441 | Rare:28 | ||||
chr1:75724248-75724845 | Common:7; Rare:212; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:76074560-76074866 | Common:2; Rare:100 | ||||
chr1:77219385-77219559 | Rare:77 | ||||
chr1:77282340-77282602 | Common:1; Rare:65 | ||||
chr1:77683014-77683109 | Common:1; Rare:16 | ||||
chr1:77683343-77683488 | Rare:40 | ||||
chr1:77701360-77701583 | Rare:58 | ||||
chr1:77759673-77760008 | Common:6; Rare:137 | ||||
chr1:77779536-77779830 | Rare:97 |