Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:85370923-85371159 | Rare:67 | ||||
chr16:86196091-86196325 | Common:1; Rare:66 | ||||
chr16:87834548-87834841 | Rare:89 | ||||
chr16:90102326-90102512 | Rare:38 | ||||
chr17:1096226-1096290 | Common:1; Rare:21 | ||||
chr17:2692572-2692863 | Common:1; Rare:119 | ||||
chr17:4530833-4531089 | Common:4; Rare:65 | ||||
chr17:4858939-4859243 | Common:1; Rare:63 | ||||
chr17:4939090-4939379 | Rare:81 | ||||
chr17:4998594-4998956 | Common:1; Rare:69 | ||||
chr17:5004345-5004645 | Rare:84; Clinvar (benign):2 | ||||
chr17:5021917-5022154 | Rare:65 | ||||
chr17:5434874-5435190 | Common:2; Rare:69 | ||||
chr17:6657861-6657940 | Common:2; Rare:11 | ||||
chr17:6666672-6666947 | Common:2; Rare:44 |