Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100905830-100906143 | Common:4; Rare:37 | ||||
chr14:100914767-100915055 | Common:3; Rare:42 | ||||
chr14:102081773-102082012 | Common:3; Rare:92 | ||||
chr15:23303503-23303785 | Common:1; Rare:29 | ||||
chr15:28589195-28589509 | Common:1; Rare:10 | ||||
chr15:29730401-29730611 | Rare:46 | ||||
chr15:34794888-34794950 | Rare:14 | ||||
chr15:39585682-39585996 | Common:3; Rare:40 | ||||
chr15:41283894-41284021 | Common:1; Rare:38 | ||||
chr15:48421672-48422021 | Common:2; Rare:86; Clinvar:6; Clinvar (benign):2 | ||||
chr15:48474289-48474559 | Common:1; Rare:60; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr15:51094638-51094988 | Common:8; Rare:94 | ||||
chr15:58771911-58772126 | Common:1; Rare:91 | ||||
chr15:65304404-65304677 | Common:5; Rare:127 | ||||
chr15:71165130-71165352 | Common:1; Rare:28 |