Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:29566964-29567297 | Rare:84 | ||||
chr17:29568505-29568740 | Common:3; Rare:76 | ||||
chr17:29582770-29582960 | Common:1; Rare:47 | ||||
chr17:29589611-29589782 | Common:3; Rare:59 | ||||
chr17:29761281-29761360 | Common:1; Rare:29 | ||||
chr17:29929006-29929289 | Common:1; Rare:52 | ||||
chr17:29930165-29930380 | Rare:65 | ||||
chr17:30477230-30477444 | Common:1; Rare:64 | ||||
chr17:30906190-30906315 | Rare:45 | ||||
chr17:30970891-30971059 | Common:2; Rare:57 | ||||
chr17:31094954-31095310 | Rare:101; Clinvar:7; Clinvar (benign):1 | ||||
chr17:31901653-31901930 | Common:2; Rare:84 | ||||
chr17:32142362-32142574 | Common:6; Rare:110 | ||||
chr17:32342123-32342262 | Rare:39 | ||||
chr17:32350002-32350194 | Rare:97 |