Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71364530-71365050 | Common:8; Rare:97 | ||||
chr10:71368618-71369018 | Common:6; Rare:89 | ||||
chr10:71377354-71377637 | Common:5; Rare:67 | ||||
chr10:71684385-71684551 | Common:5; Rare:36 | ||||
chr10:71766767-71766939 | Common:1; Rare:29 | ||||
chr10:71767734-71767998 | Common:5; Rare:56 | ||||
chr10:71805929-71806067 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:71860351-71860687 | Common:2; Rare:61 | ||||
chr10:71861005-71861108 | Common:1; Rare:12 | ||||
chr10:71868383-71868487 | Common:1; Rare:11 | ||||
chr10:71871389-71871527 | Rare:27 | ||||
chr10:71888998-71889234 | Common:5; Rare:48 | ||||
chr10:71965211-71965335 | Rare:26 | ||||
chr10:71975967-71976124 | Common:3; Rare:28 | ||||
chr10:71998978-71999105 | Common:1; Rare:16 |