Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7961456-7961787 | Common:4; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878591-8878855 | Rare:139 | ||||
chr1:9943293-9943488 | Common:2; Rare:46 | ||||
chr1:11654332-11654440 | Rare:28 | ||||
chr1:11735796-11736181 | Common:2; Rare:103 | ||||
chr1:11805905-11806217 | Common:2; Rare:83; Clinvar:1 | ||||
chr1:15305509-15305738 | Common:2; Rare:42 | ||||
chr1:15409817-15409980 | Rare:48 | ||||
chr1:19210251-19210515 | Rare:90 | ||||
chr1:19251516-19251835 | Common:6; Rare:102 | ||||
chr1:19312072-19312361 | Common:7; Rare:135 | ||||
chr1:23778340-23778451 | Common:3; Rare:56 | ||||
chr1:23825407-23825534 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:24642966-24643321 | Common:2; Rare:111 | ||||
chr1:25232462-25232633 | Rare:65 |