Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:79413038-79413135 | Common:1; Rare:18 | ||||
chr17:79810719-79810840 | Common:1; Rare:40 | ||||
chr17:80263481-80263650 | Rare:46 | ||||
chr17:80834385-80834662 | Common:4; Rare:71 | ||||
chr17:81513946-81514062 | Common:1; Rare:34 | ||||
chr18:905703-905843 | Common:2; Rare:45 | ||||
chr18:906644-906799 | Common:1; Rare:28 | ||||
chr18:3593941-3594482 | Common:3; Rare:98 | ||||
chr18:5238001-5238144 | Common:1; Rare:55 | ||||
chr18:26856334-26856656 | Common:1; Rare:68 | ||||
chr18:39841506-39841813 | Common:2; Rare:60 | ||||
chr18:46087220-46087441 | Rare:50; Clinvar (pathogenic):1 | ||||
chr18:47251635-47251774 | Rare:25 | ||||
chr18:52340762-52340772 | Rare:5 | ||||
chr18:55258365-55258803 | Common:1; Rare:74 |