Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:38869844-38870143 | Common:4; Rare:94 | ||||
chr17:39200007-39200349 | Common:2; Rare:106 | ||||
chr17:39451250-39451403 | Common:2; Rare:54 | ||||
chr17:39637024-39637176 | Common:2; Rare:44 | ||||
chr17:39688014-39688094 | Rare:26 | ||||
chr17:39927544-39927745 | Common:2; Rare:58 | ||||
chr17:40140177-40140548 | Common:5; Rare:183 | ||||
chr17:40318010-40318300 | Common:1; Rare:59 | ||||
chr17:40417811-40418186 | Rare:113 | ||||
chr17:41624457-41624902 | Common:8; Rare:126; Clinvar (benign):1 | ||||
chr17:41688651-41688894 | Common:1; Rare:78 | ||||
chr17:41689293-41689573 | Common:3; Rare:104 | ||||
chr17:41812829-41813022 | Rare:50; Clinvar:2 | ||||
chr17:41966579-41966855 | Common:2; Rare:92 | ||||
chr17:42017382-42017580 | Common:1; Rare:74 |