Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:4948942-4949010 | Rare:18 | ||||
chr17:4967800-4967913 | Rare:42 | ||||
chr17:4987640-4987795 | Rare:53 | ||||
chr17:5191838-5192106 | Common:2; Rare:88 | ||||
chr17:5419649-5419863 | Common:3; Rare:64 | ||||
chr17:5420098-5420213 | Rare:47 | ||||
chr17:5486154-5486399 | Common:4; Rare:105 | ||||
chr17:6640671-6641066 | Common:7; Rare:118 | ||||
chr17:6651542-6651747 | Common:1; Rare:68 | ||||
chr17:7012332-7012686 | Rare:119 | ||||
chr17:7484226-7484370 | Common:1; Rare:59 | ||||
chr17:7583550-7583860 | Common:1; Rare:127; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7857459-7857735 | Common:2; Rare:86 | ||||
chr17:7931826-7932243 | Common:5; Rare:115 | ||||
chr17:8248042-8248179 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):2 |