Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:80205346-80205647 | Common:4; Rare:91 | ||||
chr10:80453967-80454359 | Common:3; Rare:130 | ||||
chr10:84424769-84424983 | Rare:28 | ||||
chr10:86521719-86521967 | Rare:80 | ||||
chr10:87094868-87095240 | Common:1; Rare:88; Clinvar:2 | ||||
chr10:87504796-87505047 | Common:1; Rare:125; Clinvar (pathogenic):1 | ||||
chr10:87659626-87660193 | Common:9; Rare:154 | ||||
chr10:87660881-87660965 | Rare:12 | ||||
chr10:87818111-87818336 | Rare:77 | ||||
chr10:87863276-87863680 | Common:2; Rare:139; Clinvar:84; Clinvar (benign):9 | ||||
chr10:87864316-87864402 | Rare:19; Clinvar:2; Clinvar (benign):2 | ||||
chr10:88990506-88990898 | Common:5; Rare:110; Clinvar:1; Clinvar (benign):5 | ||||
chr10:88991062-88991438 | Common:4; Rare:80 | ||||
chr10:89301894-89302050 | Rare:32 | ||||
chr10:89327877-89328027 | Common:1; Rare:21 |