Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1971775-1972105 | Common:3; Rare:94 | ||||
chr16:2047784-2048038 | Rare:115; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2205714-2205875 | Common:4; Rare:73 | ||||
chr16:2268063-2268187 | Common:1; Rare:61 | ||||
chr16:2429154-2429478 | Common:2; Rare:104 | ||||
chr16:2459980-2460145 | Common:1; Rare:47 | ||||
chr16:2682367-2682622 | Rare:116 | ||||
chr16:2777235-2777395 | Common:2; Rare:65 | ||||
chr16:2980406-2980619 | Common:2; Rare:75 | ||||
chr16:3020064-3020400 | Rare:101 | ||||
chr16:3065207-3065424 | Common:3; Rare:59 | ||||
chr16:3134852-3135137 | Common:3; Rare:72 | ||||
chr16:3305390-3305514 | Common:1; Rare:44 | ||||
chr16:3400975-3401226 | Common:6; Rare:91 | ||||
chr16:3443452-3443725 | Common:3; Rare:89 |