Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39451249-39451375 | Common:2; Rare:43 | ||||
chr17:39688023-39688094 | Rare:22 | ||||
chr17:39927489-39927745 | Common:2; Rare:74 | ||||
chr17:40121850-40121989 | Common:2; Rare:53 | ||||
chr17:41688858-41689041 | Common:2; Rare:97 | ||||
chr17:41812589-41813007 | Common:3; Rare:88; Clinvar:5 | ||||
chr17:42111726-42112033 | Rare:80 | ||||
chr17:42535950-42536322 | Common:4; Rare:106; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr17:42577672-42577826 | Rare:72 | ||||
chr17:42609301-42609730 | Common:9; Rare:181; Clinvar (benign):2 | ||||
chr17:42682409-42682593 | Rare:43 | ||||
chr17:42773206-42773486 | Rare:64 | ||||
chr17:42798465-42798785 | Rare:110; Clinvar (pathogenic):1 | ||||
chr17:42964430-42964536 | Rare:50 | ||||
chr17:42980469-42980572 | Common:1; Rare:40 |