Variant report

Variant	rs56300927
Chromosome Location	chr3:68495036-68495037
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs6798891	1.00[AMR][1000 genomes]
rs6801600	1.00[AMR][1000 genomes]
rs73835306	1.00[AMR][1000 genomes]
rs73836901	1.00[AMR][1000 genomes]
rs73837610	1.00[AMR][1000 genomes]
rs73838717	1.00[AMR][1000 genomes]
rs73838718	1.00[AMR][1000 genomes]
rs73838720	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834721	chr3:68365963-68526394	Weak transcription Enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv1003779	chr3:68470899-68517125	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv1832396	chr3:68478762-68641509	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:68490800-68497000	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr3:68491000-68497000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr3:68494800-68495200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr3:68494800-68495200	Enhancers	HUES6 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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