Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:54269493-54269617 | Common:1; Rare:67 | ||||
chr18:54828329-54828514 | Rare:46 | ||||
chr18:57621724-57621972 | Common:3; Rare:89 | ||||
chr18:62186937-62187328 | Common:5; Rare:108 | ||||
chr18:63422377-63422643 | Common:1; Rare:69 | ||||
chr18:68715036-68715310 | Common:5; Rare:115 | ||||
chr18:70205664-70205776 | Common:3; Rare:45; Clinvar (benign):2 | ||||
chr18:74291855-74292265 | Common:4; Rare:123; Clinvar:1 | ||||
chr18:74597810-74597892 | Common:1; Rare:22 | ||||
chr18:79988404-79988661 | Common:4; Rare:97; Clinvar (pathogenic):2 | ||||
chr19:572328-572603 | Rare:139 | ||||
chr19:633505-633745 | Common:8; Rare:112 | ||||
chr19:663153-663426 | Common:2; Rare:107 | ||||
chr19:750986-751154 | Common:2; Rare:30 | ||||
chr19:893165-893411 | Common:3; Rare:77 |