Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:13418548-13418609 | Rare:15 | ||||
chr18:21241426-21241557 | Rare:31 | ||||
chr18:21740621-21740807 | Common:2; Rare:57 | ||||
chr18:22176723-22177021 | Common:1; Rare:68; Clinvar:1 | ||||
chr18:22181203-22181485 | Rare:57; Clinvar:1 | ||||
chr18:22349637-22349856 | Common:2; Rare:37 | ||||
chr18:22695018-22695131 | Common:1; Rare:16 | ||||
chr18:22711174-22711369 | Common:2; Rare:35 | ||||
chr18:24170332-24170670 | Rare:93 | ||||
chr18:34820551-34820852 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):2 | ||||
chr18:34834960-34835200 | Rare:30 | ||||
chr18:39841541-39841701 | Rare:24 | ||||
chr18:48763137-48763161 | Rare:4 | ||||
chr18:48763163-48763281 | Rare:28 | ||||
chr18:48767274-48767575 | Common:2; Rare:56 |