Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1495500-1495772 | Common:2; Rare:113 | ||||
chr16:1757595-1757701 | Common:1; Rare:17 | ||||
chr16:1896173-1896262 | Common:1; Rare:20 | ||||
chr16:2037393-2037551 | Common:3; Rare:64 | ||||
chr16:2074078-2074278 | Rare:56; Clinvar:10; Clinvar (benign):9 | ||||
chr16:2112178-2112281 | Rare:34 | ||||
chr16:2338847-2339204 | Rare:77 | ||||
chr16:2532535-2532675 | Rare:47 | ||||
chr16:2603281-2603474 | Common:2; Rare:79 | ||||
chr16:2664328-2664417 | Common:1; Rare:21 | ||||
chr16:2667215-2667395 | Common:3; Rare:48 | ||||
chr16:2669649-2669755 | Common:3; Rare:26 | ||||
chr16:2671000-2671112 | Common:3; Rare:15 | ||||
chr16:2673298-2673581 | Common:9; Rare:95 | ||||
chr16:2754953-2755247 | Rare:101 |