Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:86555180-86555329 | Rare:77 | ||||
chr16:87317337-87317516 | Common:6; Rare:70 | ||||
chr16:87383579-87383976 | Common:2; Rare:148; Clinvar (benign):1 | ||||
chr16:87765886-87766062 | Common:1; Rare:72 | ||||
chr16:88570174-88570493 | Common:1; Rare:121 | ||||
chr16:88663070-88663371 | Common:8; Rare:124 | ||||
chr16:88706186-88706548 | Common:4; Rare:159 | ||||
chr16:88856925-88857178 | Common:4; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
chr16:89217619-89217749 | Common:1; Rare:61 | ||||
chr16:89508318-89508428 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:89560541-89560742 | Rare:89 | ||||
chr16:89657641-89658095 | Common:3; Rare:237 | ||||
chr16:89686574-89686716 | Common:6; Rare:69 | ||||
chr16:89686904-89686951 | Rare:19 | ||||
chr16:89701703-89701782 | Rare:33 |