Variant report

Variant	rs7707806
Chromosome Location	chr5:167020442-167020443
allele	C/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]
rs10035359	1.00[CEU][hapmap]
rs10475852	1.00[CEU][hapmap];0.88[YRI][hapmap]
rs12515062	1.00[CEU][hapmap]
rs17068860	1.00[CEU][hapmap]
rs57629844	1.00[EUR][1000 genomes]
rs59710284	1.00[EUR][1000 genomes]
rs6862511	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6867320	1.00[EUR][1000 genomes]
rs6867682	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6869063	1.00[CEU][hapmap]
rs6882356	1.00[EUR][1000 genomes]
rs6886030	1.00[EUR][1000 genomes]
rs7730427	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7731493	1.00[CEU][hapmap]

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	nsv932627	chr5:166744408-167290959	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv883104	chr5:166971457-167037934	Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167010800-167022200	Weak transcription	Fetal Lung	lung
2	chr5:167015200-167027400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:167015600-167020800	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr5:167018800-167021000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:167019400-167036600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:167019600-167020600	Enhancers	A549	lung
7	chr5:167020400-167020600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr5:167020400-167021000	Enhancers	HSMMtube	muscle
9	chr5:167020400-167021200	Enhancers	HSMM	muscle

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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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