Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111140023-111140263 | Common:1; Rare:83 | ||||
chr1:112396051-112396262 | Common:1; Rare:65 | ||||
chr1:112619119-112619172 | Rare:24 | ||||
chr1:112619642-112619847 | Common:1; Rare:71 | ||||
chr1:112956190-112956467 | Common:5; Rare:122; Clinvar:8; Clinvar (benign):3 | ||||
chr1:113905032-113905359 | Common:3; Rare:88 | ||||
chr1:114716733-114716828 | Rare:45; Clinvar:3 | ||||
chr1:114780627-114780785 | Common:1; Rare:53 | ||||
chr1:117929585-117929811 | Common:3; Rare:66 | ||||
chr1:119140634-119140767 | Rare:42 | ||||
chr1:145823942-145824238 | Rare:104 | ||||
chr1:145859082-145859179 | Rare:22 | ||||
chr1:145927431-145927644 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
chr1:145964477-145964731 | Rare:55 | ||||
chr1:149842746-149842962 | Rare:3 |