Variant report

Variant	rs73478065
Chromosome Location	chr6:70592441-70592442
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs61267713	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6934513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73478068	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73485539	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv830682	chr6:70397851-70592883	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv886141	chr6:70590638-70694162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70588800-70597800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:70591600-70593400	Enhancers	Fetal Heart	heart
3	chr6:70591800-70592600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:70591800-70592600	Bivalent Enhancer	Primary hematopoietic stem cells	blood
5	chr6:70592000-70593000	Weak transcription	Psoas Muscle	Psoas
6	chr6:70592400-70592600	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr6:70592400-70592800	Enhancers	GM12878-XiMat	blood
8	chr6:70592400-70595200	Enhancers	Primary B cells from peripheral blood	blood

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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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