Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619109-112619236 | Rare:45 | ||||
chr1:112619643-112619847 | Common:1; Rare:70 | ||||
chr1:112956193-112956433 | Common:4; Rare:108; Clinvar:8; Clinvar (benign):3 | ||||
chr1:113073085-113073221 | Common:1; Rare:46 | ||||
chr1:113390187-113390523 | Common:1; Rare:83 | ||||
chr1:113812241-113812351 | Common:2; Rare:55 | ||||
chr1:113905025-113905339 | Common:3; Rare:84 | ||||
chr1:114581587-114581818 | Rare:101 | ||||
chr1:114716737-114716862 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
chr1:116373073-116373486 | Common:3; Rare:136 | ||||
chr1:116570978-116571162 | Common:2; Rare:54 | ||||
chr1:116754351-116754467 | Rare:34 | ||||
chr1:117060203-117060341 | Common:2; Rare:35 | ||||
chr1:117210890-117211061 | Common:2; Rare:38 | ||||
chr1:117368205-117368484 | Rare:73 |