Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87504793-87504966 | Common:1; Rare:85 | ||||
chr10:87817948-87818359 | Common:2; Rare:135 | ||||
chr10:87864242-87864538 | Common:1; Rare:73; Clinvar:17; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr10:88583292-88583364 | Rare:11 | ||||
chr10:88880175-88880549 | Common:1; Rare:79 | ||||
chr10:89332252-89332554 | Common:3; Rare:50 | ||||
chr10:89342620-89342877 | Common:3; Rare:34 | ||||
chr10:89392471-89392661 | Common:3; Rare:48 | ||||
chr10:89414672-89414785 | Common:3; Rare:54 | ||||
chr10:89643886-89644116 | Rare:47 | ||||
chr10:89701396-89701643 | Common:1; Rare:76 | ||||
chr10:91410091-91410494 | Common:5; Rare:145 | ||||
chr10:91633056-91633171 | Rare:38 | ||||
chr10:91798237-91798408 | Rare:60 | ||||
chr10:91923721-91924003 | Common:1; Rare:102 |