Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:9136486-9136855 | Rare:139 | ||||
chr18:9334482-9334818 | Common:1; Rare:86 | ||||
chr18:11908284-11908403 | Rare:31 | ||||
chr18:12702703-12703069 | Common:3; Rare:140 | ||||
chr18:12884159-12884425 | Common:4; Rare:130 | ||||
chr18:12947694-12948061 | Common:3; Rare:89 | ||||
chr18:13726484-13726726 | Common:3; Rare:90 | ||||
chr18:21600655-21600798 | Rare:37 | ||||
chr18:22169345-22169595 | Common:1; Rare:65 | ||||
chr18:22933230-22933385 | Common:2; Rare:50; Clinvar (benign):1 | ||||
chr18:23453176-23453359 | Rare:64 | ||||
chr18:23586416-23586541 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr18:24426521-24426757 | Common:5; Rare:100 | ||||
chr18:31042730-31043060 | Common:3; Rare:56 | ||||
chr18:31497963-31498246 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):3 |