Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:12702665-12703070 | Common:3; Rare:157 | ||||
chr18:12947683-12948045 | Common:2; Rare:89 | ||||
chr18:13726533-13726688 | Common:3; Rare:59 | ||||
chr18:21600699-21600852 | Rare:28 | ||||
chr18:21612194-21612418 | Common:1; Rare:68 | ||||
chr18:22933806-22933883 | Common:1; Rare:29 | ||||
chr18:35290215-35290333 | Common:1; Rare:41 | ||||
chr18:36129301-36129466 | Common:1; Rare:51 | ||||
chr18:36129817-36129928 | Rare:44 | ||||
chr18:36187408-36187546 | Common:3; Rare:55 | ||||
chr18:36828757-36829138 | Common:3; Rare:139 | ||||
chr18:46104136-46104396 | Common:3; Rare:74; Clinvar (benign):1 | ||||
chr18:49813916-49814037 | Rare:50 | ||||
chr18:50878963-50879171 | Common:4; Rare:69 | ||||
chr18:55665123-55665281 | Common:1; Rare:42 |