Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42964428-42964528 | Rare:49 | ||||
chr17:43125466-43125654 | Rare:45; Clinvar (benign):1 | ||||
chr17:43170292-43170720 | Common:3; Rare:83 | ||||
chr17:43171024-43171273 | Common:1; Rare:81 | ||||
chr17:43530415-43530508 | Rare:14 | ||||
chr17:43778868-43779076 | Rare:49 | ||||
chr17:43831848-43832029 | Rare:57 | ||||
chr17:44070612-44070918 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44111229-44111426 | Rare:55 | ||||
chr17:44123599-44123840 | Common:3; Rare:68 | ||||
chr17:44170627-44170714 | Rare:20 | ||||
chr17:44186668-44187002 | Common:1; Rare:119 | ||||
chr17:44187096-44187294 | Rare:48 | ||||
chr17:44220863-44221213 | Common:1; Rare:117 | ||||
chr17:44221262-44221427 | Rare:49 |