Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:218402615-218402714 | Rare:37 | ||||
chr2:218404146-218404389 | Rare:62 | ||||
chr2:237359211-237359443 | Rare:63; Clinvar:5; Clinvar (benign):2 | ||||
chr2:241881279-241881400 | Rare:30 | ||||
chr20:19214256-19214466 | Common:1; Rare:39 | ||||
chr20:19757959-19758276 | Common:4; Rare:112 | ||||
chr20:23633591-23633708 | Common:2; Rare:26 | ||||
chr20:24963997-24964188 | Rare:49 | ||||
chr20:25854004-25854147 | Common:3; Rare:52 | ||||
chr20:34098565-34098709 | Common:1; Rare:33 | ||||
chr20:36049955-36050247 | Common:1; Rare:63 | ||||
chr20:36050281-36050643 | Common:2; Rare:119 | ||||
chr20:38146800-38147078 | Rare:77 | ||||
chr20:45419363-45419589 | Common:2; Rare:87; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr20:47352502-47352638 | Rare:24 |