Variant report

Variant	rs11101032
Chromosome Location	chr10:50432575-50432576
allele	A/C
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:9)

rs_ID	r²[population]
rs10857441	0.81[ASN][1000 genomes]
rs10857448	0.98[ASN][1000 genomes]
rs11101027	0.92[ASN][1000 genomes]
rs11101029	0.89[ASN][1000 genomes]
rs11101057	0.93[ASN][1000 genomes]
rs17774170	0.81[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4498896	0.95[ASN][1000 genomes]
rs4838470	0.92[ASN][1000 genomes]
rs7082708	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50429400-50433200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr10:50429600-50433400	Weak transcription	Right Atrium	heart
3	chr10:50429600-50433400	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr10:50429800-50433600	Weak transcription	Right Ventricle	heart
5	chr10:50430000-50433400	Weak transcription	Left Ventricle	heart
6	chr10:50431600-50433400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:50432000-50433000	Enhancers	K562	blood

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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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