Variant report

Variant	rs1700826
Chromosome Location	chr13:76890178-76890179
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1146883	0.90[ASN][1000 genomes]
rs1146888	0.89[ASN][1000 genomes]
rs1146890	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1505141	0.91[ASN][1000 genomes]
rs17066099	0.86[ASN][1000 genomes]
rs1847629	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs1929731	0.89[ASN][1000 genomes]
rs2657128	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2777732	0.90[ASN][1000 genomes]
rs4142608	0.90[ASN][1000 genomes]
rs4142610	0.91[ASN][1000 genomes]
rs61963409	0.91[ASN][1000 genomes]
rs8001163	0.91[ASN][1000 genomes]
rs924895	0.80[ASN][1000 genomes]
rs9318421	0.84[ASN][1000 genomes]
rs9530536	0.86[ASN][1000 genomes]
rs9544243	0.90[ASN][1000 genomes]
rs9544244	0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044736	chr13:76728655-77066435	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76883200-76891200	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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