Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:86508268-86508311 | Rare:11 | ||||
chr16:86508679-86509176 | Common:4; Rare:129 | ||||
chr16:86509604-86509643 | Rare:7 | ||||
chr16:88759312-88759594 | Common:4; Rare:75 | ||||
chr16:88835501-88835672 | Common:2; Rare:32 | ||||
chr17:859301-859338 | Rare:3 | ||||
chr17:1774827-1775179 | Common:3; Rare:121; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr17:1777109-1777265 | Rare:64; Clinvar:1 | ||||
chr17:3921690-3921791 | Rare:28 | ||||
chr17:7556853-7557195 | Rare:92; Clinvar (benign):1 | ||||
chr17:7849927-7850186 | Rare:58 | ||||
chr17:7887504-7887806 | Rare:67 | ||||
chr17:8154253-8154408 | Rare:30 | ||||
chr17:8186760-8186871 | Common:2; Rare:54 | ||||
chr17:8480286-8480404 | Rare:41 |