Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44123560-44123863 | Common:3; Rare:88 | ||||
chr17:44186611-44187050 | Common:1; Rare:152 | ||||
chr17:44187161-44187274 | Rare:31 | ||||
chr17:44200123-44200524 | Common:3; Rare:172 | ||||
chr17:44220793-44221058 | Rare:88 | ||||
chr17:44221219-44221484 | Rare:76 | ||||
chr17:44222071-44222248 | Rare:39 | ||||
chr17:44308326-44308670 | Common:2; Rare:99 | ||||
chr17:44324765-44324921 | Common:1; Rare:57 | ||||
chr17:44344994-44345321 | Common:1; Rare:69; Clinvar:5; Clinvar (benign):3 | ||||
chr17:44503366-44503760 | Rare:149 | ||||
chr17:44708498-44708699 | Common:1; Rare:41 | ||||
chr17:44708728-44708924 | Common:3; Rare:64 | ||||
chr17:44899369-44899799 | Common:3; Rare:131; Clinvar:3; Clinvar (benign):1 | ||||
chr17:45051429-45051717 | Common:1; Rare:99 |