Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:667958-668164 | Common:1; Rare:72 | ||||
chr16:1678019-1678340 | Common:3; Rare:108 | ||||
chr16:1706042-1706321 | Common:2; Rare:89 | ||||
chr16:1827171-1827247 | Common:1; Rare:41 | ||||
chr16:1943193-1943497 | Common:1; Rare:89 | ||||
chr16:1971932-1972110 | Common:1; Rare:50 | ||||
chr16:2047790-2048048 | Rare:124; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268075-2268210 | Common:1; Rare:53 | ||||
chr16:2429145-2429484 | Common:3; Rare:112 | ||||
chr16:2459980-2460145 | Common:1; Rare:47 | ||||
chr16:2474970-2475149 | Rare:55 | ||||
chr16:2682367-2682653 | Rare:131 | ||||
chr16:2777116-2777388 | Common:2; Rare:113 | ||||
chr16:2980388-2980646 | Common:2; Rare:87 | ||||
chr16:3020064-3020405 | Rare:103 |