Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110007683-110008345 | Common:2; Rare:211 | ||||
chr10:110008598-110008949 | Common:6; Rare:91 | ||||
chr10:110076975-110077086 | Rare:23 | ||||
chr10:110225855-110226281 | Common:2; Rare:120 | ||||
chr10:110304851-110305143 | Common:2; Rare:96 | ||||
chr10:110567393-110567765 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):5 | ||||
chr10:110567921-110567980 | Rare:12 | ||||
chr10:110835123-110835178 | Rare:13 | ||||
chr10:110871741-110872017 | Rare:92 | ||||
chr10:110872217-110872328 | Rare:30 | ||||
chr10:110872348-110872613 | Common:1; Rare:91 | ||||
chr10:110918504-110918623 | Rare:24 | ||||
chr10:110919134-110919636 | Common:8; Rare:133 | ||||
chr10:112183672-112183857 | Common:3; Rare:65 | ||||
chr10:112376119-112376312 | Rare:37 |