Variant report

Variant	rs74095537
Chromosome Location	chr1:84784864-84784865
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs56791370	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57971598	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58909039	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59131645	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6670929	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6688872	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095544	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095547	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74095551	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7530088	0.85[AMR][1000 genomes]
rs7548576	0.96[AFR][1000 genomes];1.00[AMR][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	nsv830414	chr1:84636738-84824651	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv830426	chr1:84704924-84856229	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr1:84769200-84791400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:84777400-84791200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr1:84780200-84791400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr1:84782800-84785800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:84783000-84791200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr1:84784600-84785800	Enhancers	NHEK	skin
7	chr1:84784800-84785000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:84784800-84785600	Enhancers	A549	lung
9	chr1:84784800-84785800	Enhancers	HMEC	breast
10	chr1:84784800-84786000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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