Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:29582771-29582930 | Common:1; Rare:40 | ||||
chr17:32350038-32350191 | Rare:80 | ||||
chr17:34961440-34961540 | Rare:39 | ||||
chr17:35242910-35243087 | Rare:60 | ||||
chr17:36534866-36535020 | Common:2; Rare:68 | ||||
chr17:37406820-37406924 | Rare:38 | ||||
chr17:39688042-39688098 | Rare:16 | ||||
chr17:41688854-41689030 | Common:2; Rare:96 | ||||
chr17:41812601-41813010 | Common:3; Rare:86; Clinvar:5 | ||||
chr17:42552909-42552925 | Rare:7 | ||||
chr17:42609307-42609723 | Common:8; Rare:176; Clinvar (benign):2 | ||||
chr17:42682429-42682585 | Rare:37 | ||||
chr17:42798682-42798780 | Rare:28 | ||||
chr17:43020169-43020319 | Rare:29 | ||||
chr17:43125362-43125714 | Rare:77; Clinvar:3; Clinvar (benign):2 |