Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:87589973-87590141 | Common:1; Rare:65; Clinvar (benign):1 | ||||
chr6:159789632-159789826 | Rare:66 | ||||
chr7:29563654-29563885 | Common:1; Rare:59 | ||||
chr7:30594769-30594899 | Common:1; Rare:61; Clinvar:4; Clinvar (benign):3 | ||||
chr7:42932160-42932379 | Rare:83 | ||||
chr7:99408824-99408972 | Common:1; Rare:46 | ||||
chr8:60516766-60516987 | Common:3; Rare:83 | ||||
chr8:124539082-124539178 | Common:1; Rare:51; Clinvar (benign):5 | ||||
chr8:143018435-143018499 | Rare:16 | ||||
chr9:129835255-129835449 | Common:2; Rare:71 | ||||
chr9:133356458-133356558 | Common:1; Rare:42; Clinvar (benign):2 | ||||
chr9:137205638-137205665 | Rare:10 | ||||
chrM:8048-8391 | |||||
chrM:9168-9225 | |||||
chrM:10185-10472 |