Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:78187042-78187364 | Common:3; Rare:101 | ||||
chr17:81666554-81666763 | Common:1; Rare:91 | ||||
chr17:81683728-81684034 | Common:4; Rare:149 | ||||
chr18:2571443-2571604 | Rare:52 | ||||
chr18:9334488-9334879 | Common:1; Rare:100 | ||||
chr18:12702703-12703065 | Common:2; Rare:139 | ||||
chr18:23586434-23586528 | Common:2; Rare:48; Clinvar:3; Clinvar (benign):1 | ||||
chr18:35290234-35290333 | Common:1; Rare:31 | ||||
chr18:36828958-36829131 | Common:3; Rare:63 | ||||
chr18:49813835-49814026 | Common:1; Rare:79 | ||||
chr18:62187026-62187270 | Common:3; Rare:63 | ||||
chr18:63367138-63367328 | Common:1; Rare:68 | ||||
chr18:63422403-63422708 | Common:2; Rare:86 | ||||
chr19:572328-572603 | Rare:139 | ||||
chr19:1438255-1438438 | Rare:68 |