Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:63550190-63550608 | Common:3; Rare:89 | ||||
chr17:63700036-63700341 | Common:1; Rare:78 | ||||
chr17:63701144-63701238 | Rare:24 | ||||
chr17:63741765-63741930 | Common:2; Rare:60 | ||||
chr17:63773466-63773867 | Common:2; Rare:129 | ||||
chr17:63774080-63774322 | Common:8; Rare:113 | ||||
chr17:63827057-63827503 | Common:5; Rare:129 | ||||
chr17:64130010-64130368 | Common:6; Rare:92 | ||||
chr17:64263228-64263447 | Common:2; Rare:83 | ||||
chr17:64497014-64497136 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):2 | ||||
chr17:64506229-64506785 | Common:8; Rare:213 | ||||
chr17:64662297-64662436 | Common:1; Rare:64 | ||||
chr17:65056520-65056965 | Common:5; Rare:184 | ||||
chr17:65137265-65137474 | Common:1; Rare:67 | ||||
chr17:67245147-67245276 | Rare:39 |