Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:13731109-13731195 | Rare:17 | ||||
chr1:13749191-13749460 | Common:2; Rare:97 | ||||
chr1:14598391-14598691 | Common:1; Rare:90 | ||||
chr1:15410043-15410279 | Common:2; Rare:71 | ||||
chr1:15526600-15526924 | Common:2; Rare:105 | ||||
chr1:15617188-15617451 | Common:2; Rare:73 | ||||
chr1:15729689-15729906 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
chr1:15946189-15946442 | Common:1; Rare:66 | ||||
chr1:16352365-16352591 | Common:3; Rare:120 | ||||
chr1:16440617-16440852 | Common:1; Rare:88 | ||||
chr1:16455693-16455892 | Common:1; Rare:53 | ||||
chr1:16613468-16613687 | Common:2; Rare:1 | ||||
chr1:17053953-17054353 | Common:3; Rare:127; Clinvar:16; Clinvar (benign):11 | ||||
chr1:17119435-17119602 | Rare:43 | ||||
chr1:17439662-17439901 | Rare:80 |