Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:52652543-52652939 | Common:3; Rare:116 | ||||
chr13:60163771-60164118 | Common:2; Rare:88 | ||||
chr13:60396959-60397092 | Rare:29 | ||||
chr13:72727591-72727972 | Common:4; Rare:147 | ||||
chr13:72781843-72782198 | Common:1; Rare:137 | ||||
chr13:75549409-75549860 | Common:8; Rare:120 | ||||
chr13:75636033-75636366 | Common:2; Rare:76 | ||||
chr13:76991975-76992181 | Common:2; Rare:96; Clinvar:17; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
chr13:79405784-79405867 | Rare:33 | ||||
chr13:79406227-79406309 | Common:1; Rare:27 | ||||
chr13:79481152-79481467 | Common:1; Rare:135 | ||||
chr13:93227325-93227354 | Rare:5 | ||||
chr13:94601646-94601930 | Common:3; Rare:82 | ||||
chr13:95676900-95677197 | Common:3; Rare:108 | ||||
chr13:96053335-96053550 | Common:2; Rare:97 |