Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:76537904-76537953 | Rare:15 | ||||
chr17:78187045-78187364 | Common:3; Rare:100 | ||||
chr17:81683792-81684052 | Common:4; Rare:117 | ||||
chr17:81703292-81703551 | Common:2; Rare:79; Clinvar (benign):2 | ||||
chr17:81891404-81891785 | Common:3; Rare:150 | ||||
chr17:82273691-82273778 | Rare:23 | ||||
chr18:13726509-13726714 | Common:3; Rare:79 | ||||
chr18:36129762-36129924 | Common:1; Rare:59 | ||||
chr18:36187428-36187528 | Common:2; Rare:43 | ||||
chr18:36828765-36829120 | Common:1; Rare:126 | ||||
chr18:49813826-49814039 | Common:1; Rare:88 | ||||
chr18:62186991-62187285 | Common:4; Rare:82 | ||||
chr18:77087523-77087629 | Common:2; Rare:24 | ||||
chr19:1026504-1026633 | Rare:50 | ||||
chr19:2328562-2328696 | Rare:66 |