Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8487426-8487772 | Rare:92; Clinvar (benign):1 | ||||
chr17:8490729-8490815 | Rare:19 | ||||
chr17:8504692-8505081 | Common:1; Rare:77 | ||||
chr17:8506450-8506674 | Rare:43 | ||||
chr17:8512430-8512811 | Common:2; Rare:67 | ||||
chr17:8513536-8513923 | Common:2; Rare:89 | ||||
chr17:8513932-8514179 | Rare:56 | ||||
chr17:8549813-8549858 | Common:2; Rare:14 | ||||
chr17:9228535-9228621 | Common:1; Rare:13 | ||||
chr17:16037579-16037718 | Rare:21 | ||||
chr17:16061853-16062090 | Common:1; Rare:61 | ||||
chr17:16103556-16103630 | Rare:11 | ||||
chr17:16438854-16439060 | Common:1; Rare:60 | ||||
chr17:16441345-16441504 | Rare:44 | ||||
chr17:17836180-17836429 | Common:3; Rare:67 |