Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1964437-1965061 | Common:18; Rare:268 | ||||
chr16:1971932-1972079 | Common:1; Rare:41 | ||||
chr16:2047795-2048043 | Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268066-2268497 | Common:4; Rare:154 | ||||
chr16:2429145-2429447 | Common:2; Rare:94 | ||||
chr16:2459970-2460112 | Rare:35 | ||||
chr16:2474976-2475136 | Rare:51 | ||||
chr16:2513645-2514005 | Rare:122 | ||||
chr16:2682352-2682622 | Rare:127 | ||||
chr16:2777235-2777415 | Common:3; Rare:72 | ||||
chr16:2883090-2883324 | Common:3; Rare:89 | ||||
chr16:2911772-2912018 | Common:3; Rare:86 | ||||
chr16:3065207-3065403 | Common:3; Rare:54 | ||||
chr16:3112454-3112605 | Rare:40 | ||||
chr16:3134829-3135153 | Common:3; Rare:91 |