Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:44536863-44537464 | Common:3; Rare:215 | ||||
chr15:44663556-44663861 | Rare:150; Clinvar:11; Clinvar (benign):6 | ||||
chr15:44728842-44729189 | Common:1; Rare:71 | ||||
chr15:45023052-45023237 | Common:3; Rare:50 | ||||
chr15:45187512-45187716 | Rare:46 | ||||
chr15:45200482-45200658 | Common:1; Rare:52 | ||||
chr15:45201084-45201200 | Common:2; Rare:56 | ||||
chr15:45378477-45378658 | Common:4; Rare:51; Clinvar:1; Clinvar (benign):4 | ||||
chr15:45402219-45402360 | Common:2; Rare:41 | ||||
chr15:45587061-45587660 | Common:2; Rare:170; Clinvar:7; Clinvar (benign):3 | ||||
chr15:45587696-45587838 | Common:2; Rare:37 | ||||
chr15:47184007-47184397 | Common:2; Rare:120 | ||||
chr15:47185140-47185219 | Rare:17 | ||||
chr15:47185293-47185608 | Rare:61 | ||||
chr15:48178075-48178488 | Common:1; Rare:122 |