Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6640660-6641198 | Common:8; Rare:176 | ||||
chr17:7012326-7012681 | Rare:121 | ||||
chr17:7219821-7219949 | Common:3; Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
chr17:7242270-7242624 | Common:1; Rare:109 | ||||
chr17:7251955-7252286 | Common:1; Rare:129 | ||||
chr17:7307929-7308077 | Common:1; Rare:36 | ||||
chr17:7479479-7479688 | Common:1; Rare:35 | ||||
chr17:7484109-7484370 | Common:1; Rare:87 | ||||
chr17:7583510-7583872 | Common:1; Rare:142; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7627807-7627969 | Common:2; Rare:53 | ||||
chr17:7857455-7857725 | Common:2; Rare:87 | ||||
chr17:7857869-7858003 | Rare:50 | ||||
chr17:7931898-7932241 | Common:5; Rare:93 | ||||
chr17:10697505-10697639 | Common:3; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr17:11997441-11997607 | Rare:55 |