Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111140046-111140269 | Common:1; Rare:80 | ||||
chr1:111739348-111739704 | Common:3; Rare:100 | ||||
chr1:111755505-111755744 | Common:3; Rare:82 | ||||
chr1:112395937-112396262 | Common:2; Rare:105 | ||||
chr1:112619109-112619242 | Rare:47 | ||||
chr1:112619634-112619883 | Common:2; Rare:88 | ||||
chr1:112674427-112674768 | Common:2; Rare:68 | ||||
chr1:112956150-112956442 | Common:4; Rare:128; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073081-113073247 | Common:1; Rare:60 | ||||
chr1:113812260-113812551 | Common:2; Rare:119 | ||||
chr1:113904761-113904967 | Common:1; Rare:57; Clinvar (benign):2 | ||||
chr1:113905026-113905392 | Common:5; Rare:101 | ||||
chr1:114716674-114716862 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):2 | ||||
chr1:117929568-117929800 | Common:2; Rare:69 | ||||
chr1:119140634-119140735 | Rare:29 |