Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:52652543-52652951 | Common:3; Rare:123 | ||||
chr13:52653085-52653150 | Rare:25 | ||||
chr13:60163802-60164118 | Common:2; Rare:79 | ||||
chr13:60396307-60396505 | Common:2; Rare:75 | ||||
chr13:60396731-60397086 | Rare:90 | ||||
chr13:60397173-60397380 | Common:4; Rare:76 | ||||
chr13:72727556-72727972 | Common:7; Rare:164 | ||||
chr13:72781616-72781626 | Rare:4 | ||||
chr13:72781699-72782198 | Common:1; Rare:191 | ||||
chr13:73058650-73059060 | Common:2; Rare:143 | ||||
chr13:75482392-75482488 | Common:1; Rare:24 | ||||
chr13:75549460-75549860 | Common:8; Rare:103 | ||||
chr13:76992047-76992194 | Common:1; Rare:69; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
chr13:77027136-77027249 | Common:5; Rare:39 | ||||
chr13:77327030-77327161 | Rare:67 |