Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:68054040-68054322 | Rare:76 | ||||
chr15:68820733-68821090 | Rare:106 | ||||
chr15:69160342-69160639 | Common:3; Rare:89 | ||||
chr15:69414268-69414448 | Rare:67 | ||||
chr15:69452711-69452896 | Common:4; Rare:83 | ||||
chr15:70763438-70763694 | Common:2; Rare:90 | ||||
chr15:70854101-70854289 | Rare:62 | ||||
chr15:72375958-72376124 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72686147-72686222 | Common:2; Rare:29; Clinvar:2; Clinvar (benign):2 | ||||
chr15:74461107-74461416 | Rare:86 | ||||
chr15:74540960-74541257 | Common:3; Rare:102 | ||||
chr15:74873313-74873484 | Common:6; Rare:51 | ||||
chr15:75335967-75336089 | Common:1; Rare:53 | ||||
chr15:75625624-75625862 | Common:1; Rare:56 | ||||
chr15:75640175-75640376 | Common:1; Rare:66 |