Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:79598947-79598957 | Rare:3 | ||||
chr16:84730567-84730710 | Common:3; Rare:32 | ||||
chr16:86579126-86579419 | Common:2; Rare:109; Clinvar:1 | ||||
chr16:86669891-86670154 | Common:2; Rare:69 | ||||
chr16:87381433-87381593 | Rare:32 | ||||
chr16:87855971-87856190 | Common:2; Rare:56 | ||||
chr16:87856285-87856369 | Rare:22 | ||||
chr16:88268232-88268494 | Common:4; Rare:49 | ||||
chr16:88883290-88883392 | Rare:38 | ||||
chr17:301871-302106 | Common:3; Rare:55 | ||||
chr17:4586260-4586416 | Common:2; Rare:15 | ||||
chr17:4953048-4953340 | Common:5; Rare:86; Clinvar (benign):6 | ||||
chr17:4999649-4999969 | Common:1; Rare:73; Clinvar (benign):1 | ||||
chr17:5000024-5000232 | Common:2; Rare:41 | ||||
chr17:5000352-5000645 | Rare:77 |