Variant report

Variant	rs73330120
Chromosome Location	chr8:125084309-125084310
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10087218	1.00[ASN][1000 genomes]
rs28413919	1.00[ASN][1000 genomes]
rs28733843	0.88[ASN][1000 genomes]
rs28758377	1.00[ASN][1000 genomes]
rs56813553	0.94[ASN][1000 genomes]
rs57265559	1.00[ASN][1000 genomes]
rs57874567	1.00[ASN][1000 genomes]
rs58562578	1.00[ASN][1000 genomes]
rs59645347	1.00[ASN][1000 genomes]
rs60486597	1.00[ASN][1000 genomes]
rs60939722	1.00[ASN][1000 genomes]
rs73328367	0.88[ASN][1000 genomes]
rs73328371	0.88[ASN][1000 genomes]
rs73328390	0.94[ASN][1000 genomes]
rs73328395	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs73328397	0.94[ASN][1000 genomes]
rs73330111	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73330116	1.00[ASN][1000 genomes]
rs73330123	1.00[ASN][1000 genomes]
rs73330135	1.00[ASN][1000 genomes]
rs73330139	1.00[ASN][1000 genomes]
rs73330143	0.89[ASN][1000 genomes]
rs73330144	1.00[ASN][1000 genomes]
rs73330146	1.00[ASN][1000 genomes]
rs73330149	1.00[ASN][1000 genomes]
rs73330154	1.00[ASN][1000 genomes]
rs73330160	1.00[ASN][1000 genomes]
rs73330174	1.00[ASN][1000 genomes]
rs73330176	1.00[ASN][1000 genomes]
rs73330180	1.00[ASN][1000 genomes]
rs73330182	1.00[ASN][1000 genomes]
rs73332219	1.00[ASN][1000 genomes]
rs73703924	1.00[ASN][1000 genomes]
rs73703927	1.00[ASN][1000 genomes]
rs73703948	1.00[ASN][1000 genomes]
rs7817061	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv6375	chr8:125056543-125087258	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv612144	chr8:125057728-125206503	Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1023183	chr8:125060532-125206445	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv948556	chr8:125067187-125204721	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 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	chr8:125074800-125095400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr8:125076800-125121800	Weak transcription	Fetal Stomach	stomach
3	chr8:125080200-125090000	Weak transcription	Left Ventricle	heart
4	chr8:125082400-125089200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr8:125083200-125084400	Strong transcription	Stomach Mucosa	stomach
6	chr8:125083400-125084600	Enhancers	K562	blood
7	chr8:125083600-125084400	Strong transcription	Gastric	stomach

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Input of quick search could be:

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

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