Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4143028-4143244 | Rare:69 | ||||
chr17:4143605-4143735 | Common:4; Rare:76 | ||||
chr17:4555326-4555503 | Common:3; Rare:81 | ||||
chr17:4704108-4704260 | Rare:80 | ||||
chr17:4739747-4739939 | Common:1; Rare:38 | ||||
chr17:4806996-4807201 | Common:4; Rare:65 | ||||
chr17:4903054-4903283 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr17:4939906-4940338 | Common:2; Rare:127 | ||||
chr17:4950452-4950596 | Rare:32 | ||||
chr17:4956340-4956594 | Rare:64 | ||||
chr17:4967154-4967406 | Common:2; Rare:56 | ||||
chr17:4967725-4967843 | Rare:58 | ||||
chr17:4967948-4967979 | Rare:12 | ||||
chr17:4987635-4987765 | Common:1; Rare:49 | ||||
chr17:5007034-5007310 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):2 |