Variant report

Variant	rs73486634
Chromosome Location	chr9:100569280-100569281
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10983853	0.88[EUR][1000 genomes]
rs10983855	0.88[EUR][1000 genomes]
rs10983871	0.88[EUR][1000 genomes]
rs10983889	0.83[EUR][1000 genomes]
rs10983920	0.85[ASN][1000 genomes]
rs10983958	0.83[EUR][1000 genomes]
rs10983959	0.83[EUR][1000 genomes]
rs1822416	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2401638	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs41274260	0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57541835	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73486628	1.00[AMR][1000 genomes]
rs73486635	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7859751	0.82[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	nsv1043753	chr9:100458109-100599265	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv893611	chr9:100561055-100739888	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:100566200-100570800	Weak transcription	Right Atrium	heart
2	chr9:100566400-100569600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:100566400-100570000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:100566600-100574000	Weak transcription	Pancreas	Pancrea
5	chr9:100566800-100569400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:100566800-100570600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr9:100567000-100571800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:100568800-100575000	Enhancers	HMEC	breast
9	chr9:100568800-100575000	Enhancers	NHEK	skin
10	chr9:100569000-100574800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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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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