Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:107868357-107868463 | Rare:31 | ||||
chr13:109494932-109495159 | Common:1; Rare:38 | ||||
chr13:111410789-111410974 | Rare:33 | ||||
chr13:111893273-111893434 | Rare:38 | ||||
chr13:112069590-112070003 | Common:2; Rare:89 | ||||
chr13:113216247-113216373 | Rare:21 | ||||
chr13:114077942-114078110 | Common:2; Rare:36 | ||||
chr14:20682438-20682522 | Rare:17 | ||||
chr14:20682774-20682781 | Rare:1 | ||||
chr14:21109848-21110033 | Rare:29 | ||||
chr14:22930486-22930743 | Common:2; Rare:53 | ||||
chr14:23430803-23430928 | Common:1; Rare:23; Clinvar (benign):5 | ||||
chr14:23483386-23483456 | Common:1; Rare:8 | ||||
chr14:23549210-23549357 | Common:1; Rare:37 | ||||
chr14:23584310-23584474 | Common:1; Rare:47 |