Variant report

Variant	rs11693673
Chromosome Location	chr2:73355114-73355115
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10865396	0.85[ASN][1000 genomes]
rs11126389	0.85[ASN][1000 genomes]
rs11126390	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11686557	0.80[ASN][1000 genomes]
rs12614059	0.83[ASN][1000 genomes]
rs13018842	0.85[ASN][1000 genomes]
rs13019020	0.97[ASN][1000 genomes]
rs2060002	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35131031	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4852908	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7567413	0.98[ASN][1000 genomes]
rs7570459	0.98[ASN][1000 genomes]
rs7596830	0.98[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	nsv1006801	chr2:73305056-73431711	Weak transcription Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr2:73345600-73356200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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

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