Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18253330-18253661 | Rare:117 | ||||
chr17:18258676-18258811 | Common:1; Rare:46 | ||||
chr17:18260411-18260678 | Rare:78 | ||||
chr17:18314910-18315326 | Common:1; Rare:116 | ||||
chr17:18856152-18856375 | Common:1; Rare:40 | ||||
chr17:19362665-19362773 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr17:19377905-19378043 | Common:1; Rare:31 | ||||
chr17:19378162-19378530 | Common:2; Rare:90 | ||||
chr17:19648611-19648810 | Common:2; Rare:65 | ||||
chr17:19977799-19977932 | Common:1; Rare:44 | ||||
chr17:21214144-21214368 | Common:2; Rare:102 | ||||
chr17:27293958-27294140 | Common:1; Rare:78 | ||||
chr17:27560049-27560393 | Common:2; Rare:69 | ||||
chr17:28318937-28319258 | Common:3; Rare:116 | ||||
chr17:28335371-28335850 | Common:1; Rare:113 |