Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:36951679-36951793 | Common:1; Rare:21; Clinvar (benign):2 | ||||
chr20:37178891-37179179 | Rare:83 | ||||
chr20:38033416-38033767 | Common:2; Rare:102 | ||||
chr20:38165194-38165376 | Common:1; Rare:65 | ||||
chr20:43457782-43457907 | Rare:52 | ||||
chr20:44210751-44211102 | Common:5; Rare:122 | ||||
chr20:44885602-44885812 | Common:4; Rare:78 | ||||
chr20:44966328-44966557 | Common:1; Rare:92 | ||||
chr20:45406418-45406717 | Rare:76 | ||||
chr20:45791916-45792005 | Common:1; Rare:35 | ||||
chr20:45857355-45857591 | Common:3; Rare:58 | ||||
chr20:45891227-45891387 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
chr20:46364386-46364510 | Rare:48 | ||||
chr20:46513532-46513665 | Common:3; Rare:52 | ||||
chr20:49046156-49046354 | Common:3; Rare:59 |