Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:78378588-78378687 | Common:1; Rare:44 | ||||
chr17:78723281-78723412 | Rare:29 | ||||
chr17:78723482-78723606 | Rare:38 | ||||
chr17:78782221-78782549 | Common:6; Rare:102 | ||||
chr17:78840740-78841114 | Common:2; Rare:141 | ||||
chr17:79009727-79009935 | Common:8; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
chr17:79183416-79183566 | Common:1; Rare:39 | ||||
chr17:79183678-79183735 | Rare:23 | ||||
chr17:79796999-79797420 | Common:1; Rare:148 | ||||
chr17:79950796-79951023 | Common:2; Rare:36 | ||||
chr17:80035837-80036031 | Common:1; Rare:67 | ||||
chr17:80036517-80036721 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
chr17:80036973-80037131 | Rare:52 | ||||
chr17:80101350-80101668 | Common:5; Rare:135; Clinvar (benign):5 | ||||
chr17:80146971-80147383 | Common:10; Rare:182 |