Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:69502202-69502274 | Rare:16 | ||||
chr17:69502279-69502406 | Rare:22 | ||||
chr17:70169252-70169554 | Common:1; Rare:79 | ||||
chr17:72120717-72121212 | Rare:116; Clinvar:2 | ||||
chr17:73092625-73092858 | Common:1; Rare:53 | ||||
chr17:73164835-73165082 | Common:2; Rare:70 | ||||
chr17:73192485-73193291 | Common:21; Rare:273; Clinvar:8; Clinvar (benign):1 | ||||
chr17:73232109-73232729 | Common:4; Rare:239 | ||||
chr17:73233130-73233175 | Rare:12 | ||||
chr17:73309893-73310047 | Rare:28 | ||||
chr17:73311071-73311105 | Rare:8 | ||||
chr17:73311940-73312326 | Rare:100 | ||||
chr17:74203527-74203789 | Common:3; Rare:82 | ||||
chr17:74213242-74213655 | Common:4; Rare:96 | ||||
chr17:74430634-74430959 | Common:4; Rare:79 |