Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28722872-28722923 | Rare:14 | ||||
chr17:28728643-28728838 | Rare:71; Clinvar (benign):1 | ||||
chr17:28897534-28897634 | Rare:37 | ||||
chr17:28897698-28897790 | Common:1; Rare:26 | ||||
chr17:29140362-29140490 | Common:3; Rare:40 | ||||
chr17:29293822-29293879 | Rare:17 | ||||
chr17:29293926-29293986 | Rare:15 | ||||
chr17:29294042-29294327 | Common:2; Rare:126 | ||||
chr17:29566086-29566219 | Rare:41 | ||||
chr17:29566246-29566368 | Rare:42 | ||||
chr17:29566964-29567305 | Rare:87 | ||||
chr17:29567999-29568132 | Rare:20 | ||||
chr17:29568450-29568740 | Common:4; Rare:99 | ||||
chr17:29930171-29930309 | Rare:52 | ||||
chr17:30477273-30477464 | Rare:60 |