Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10693740-10693857 | Rare:36 | ||||
chr1:11012202-11012362 | Rare:40 | ||||
chr1:11012587-11012725 | Common:1; Rare:41; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11013001-11013178 | Rare:60 | ||||
chr1:11059952-11060385 | Common:3; Rare:139 | ||||
chr1:11060415-11060451 | Rare:8 | ||||
chr1:11099331-11099471 | Rare:33 | ||||
chr1:11099749-11100041 | Common:3; Rare:114 | ||||
chr1:11262434-11262914 | Common:3; Rare:138 | ||||
chr1:11272921-11273320 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273695-11273727 | Rare:5 | ||||
chr1:11273980-11274010 | Rare:10; Clinvar (benign):1 | ||||
chr1:11479125-11479176 | Common:3; Rare:22 | ||||
chr1:11664586-11664798 | Common:1; Rare:52 | ||||
chr1:11664945-11665054 | Common:3; Rare:19 |