Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:157382469-157382662 | Rare:45 | ||||
chr5:157574617-157574837 | Common:4; Rare:55 | ||||
chr5:159100301-159100517 | Common:3; Rare:68 | ||||
chr5:172656705-172656775 | Common:1; Rare:19 | ||||
chr5:172770584-172770675 | Rare:27 | ||||
chr5:180831567-180831669 | Common:2; Rare:43 | ||||
chr6:24714317-24714614 | Common:3; Rare:68 | ||||
chr6:26521790-26522070 | Common:1; Rare:54 | ||||
chr6:32894576-32894782 | Common:8; Rare:57 | ||||
chr6:33425665-33425831 | Common:1; Rare:42; Clinvar (benign):1 | ||||
chr6:43172294-43172414 | Common:1; Rare:20 | ||||
chr6:44249412-44249834 | Common:1; Rare:113 | ||||
chr6:53793667-53793785 | Common:2; Rare:18 | ||||
chr6:57961347-57961628 | Common:2; Rare:91 | ||||
chr6:73518352-73518849 | Common:1; Rare:143 |