Variant report

Variant	rs3919476
Chromosome Location	chr7:16327408-16327409
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16325178..16329293-chr7:16335508..16338297,3	K562	blood:
2	chr7:16322591..16325161-chr7:16326295..16328787,3	K562	blood:
3	chr7:16317326..16322342-chr7:16324212..16328939,6	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10950610	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10950613	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10950614	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10950616	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11508469	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12155021	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12531973	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12533801	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12539671	0.97[ASN][1000 genomes]
rs12540311	1.00[ASN][1000 genomes]
rs12666346	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12666868	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13437646	0.82[ASN][1000 genomes]
rs17169417	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17169426	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1921839	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4001474	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4463323	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4615457	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55750250	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55966090	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56327615	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56815850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57026722	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57381059	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58553783	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs58877550	0.82[EUR][1000 genomes]
rs61227640	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61391935	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72506102	0.91[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73304492	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73306417	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73684129	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73684130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7785481	0.82[ASN][1000 genomes]
rs7804654	0.80[ASN][1000 genomes]
rs9648214	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv948950	chr7:16168925-16395434	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	esv2757214	chr7:16236162-16334228	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv2759514	chr7:16236162-16527390	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
5	nsv1022388	chr7:16251992-16431864	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1022814	chr7:16262300-16339988	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv2758105	chr7:16272822-16527390	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16312400-16332800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:16313600-16348200	Weak transcription	Gastric	stomach
3	chr7:16320600-16329200	ZNF genes & repeats	K562	blood

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