Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5419628-5419854 | Common:3; Rare:75 | ||||
chr17:5420098-5420255 | Rare:65 | ||||
chr17:5433312-5433623 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
chr17:5486157-5486581 | Common:5; Rare:143 | ||||
chr17:5486801-5486902 | Common:4; Rare:29 | ||||
chr17:6640645-6641226 | Common:8; Rare:196 | ||||
chr17:6651553-6651720 | Common:1; Rare:63 | ||||
chr17:7012317-7012720 | Rare:132 | ||||
chr17:7219745-7219949 | Common:3; Rare:84; Clinvar:5; Clinvar (benign):1 | ||||
chr17:7223773-7224361 | Rare:196; Clinvar:16; Clinvar (benign):12; Clinvar (pathogenic):17 | ||||
chr17:7251963-7252252 | Common:1; Rare:112 | ||||
chr17:7262452-7262726 | Common:3; Rare:66 | ||||
chr17:7307876-7308037 | Common:1; Rare:41 | ||||
chr17:7308731-7308971 | Rare:54 | ||||
chr17:7351626-7351743 | Rare:20 |