Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:38702311-38702479 | Rare:57 | ||||
chr17:39209821-39209900 | Rare:17 | ||||
chr17:40108220-40108364 | Rare:28 | ||||
chr17:40120723-40120902 | Rare:36 | ||||
chr17:42329428-42329643 | Common:1; Rare:55; Clinvar (benign):3 | ||||
chr17:42422614-42422792 | Rare:73; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:42759815-42760043 | Rare:51 | ||||
chr17:42851850-42852165 | Rare:119 | ||||
chr17:43010860-43011057 | Rare:31 | ||||
chr17:43388301-43388443 | Rare:32 | ||||
chr17:45149859-45150036 | Rare:36 | ||||
chr17:45585164-45585330 | Rare:22 | ||||
chr17:47100248-47100422 | Common:1; Rare:47 | ||||
chr17:47605210-47605434 | Rare:42 | ||||
chr17:48578386-48578426 | Common:1; Rare:11 |