Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8878578-8878860 | Rare:148 | ||||
chr1:9942963-9943010 | Common:1; Rare:12 | ||||
chr1:9943025-9943133 | Rare:29 | ||||
chr1:9943291-9943488 | Common:2; Rare:47 | ||||
chr1:10398903-10399103 | Common:2; Rare:78 | ||||
chr1:11262495-11262828 | Common:2; Rare:100 | ||||
chr1:11273430-11273510 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chr1:11654787-11654904 | Common:2; Rare:37 | ||||
chr1:12617226-12617322 | Rare:31 | ||||
chr1:12618189-12618444 | Common:1; Rare:57 | ||||
chr1:13749191-13749451 | Common:2; Rare:92 | ||||
chr1:15758743-15758817 | Common:1; Rare:18 | ||||
chr1:16352424-16352615 | Common:3; Rare:101 | ||||
chr1:16440594-16440759 | Rare:49 | ||||
chr1:17053960-17054331 | Common:3; Rare:117; Clinvar:16; Clinvar (benign):10 |