Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:54357872-54358074 | Common:7; Rare:56 | ||||
chr18:62186960-62187310 | Common:5; Rare:97 | ||||
chr18:63367158-63367304 | Common:1; Rare:50 | ||||
chr18:68715033-68715254 | Common:3; Rare:102 | ||||
chr18:74291942-74292272 | Common:4; Rare:91 | ||||
chr18:74597579-74597910 | Common:2; Rare:89 | ||||
chr18:75209054-75209492 | Common:3; Rare:131 | ||||
chr18:77087147-77087271 | Common:5; Rare:41 | ||||
chr18:79988306-79988655 | Common:3; Rare:117; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr19:489015-489206 | Common:7; Rare:60 | ||||
chr19:572322-572603 | Rare:139 | ||||
chr19:633502-633724 | Common:8; Rare:111 | ||||
chr19:663153-663438 | Common:2; Rare:116 | ||||
chr19:1103770-1104115 | Common:6; Rare:146 | ||||
chr19:1269143-1269355 | Common:2; Rare:81 |