Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:93702940-93703028 | Rare:12 | ||||
chr10:93757704-93758099 | Common:1; Rare:67; Clinvar:4; Clinvar (benign):1 | ||||
chr10:93893905-93894007 | Common:1; Rare:45 | ||||
chr10:93993741-93994100 | Common:5; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr10:94362892-94363046 | Common:3; Rare:62 | ||||
chr10:94545679-94545862 | Common:3; Rare:63 | ||||
chr10:95561320-95561556 | Common:3; Rare:65 | ||||
chr10:95693906-95694207 | Common:5; Rare:87; Clinvar (benign):1 | ||||
chr10:95907756-95907927 | Common:2; Rare:45 | ||||
chr10:95908121-95908162 | Rare:9 | ||||
chr10:96129979-96130530 | Common:5; Rare:184 | ||||
chr10:97426037-97426308 | Common:2; Rare:125 | ||||
chr10:97445975-97446229 | Rare:67 | ||||
chr10:97498385-97498569 | Common:2; Rare:69 | ||||
chr10:97633434-97633637 | Common:2; Rare:51 |