Variant report

Variant	rs61913473
Chromosome Location	chr12:10079941-10079942
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11610998	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11612095	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11612832	0.94[EUR][1000 genomes]
rs17204888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57926493	0.94[EUR][1000 genomes]
rs59775298	0.94[EUR][1000 genomes]
rs59789233	0.94[EUR][1000 genomes]
rs60732080	0.94[EUR][1000 genomes]
rs60806917	0.94[EUR][1000 genomes]
rs61913469	0.84[ASN][1000 genomes]
rs61913470	0.84[ASN][1000 genomes]
rs61913476	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7967565	0.94[EUR][1000 genomes]
rs7968634	0.94[EUR][1000 genomes]
rs7971846	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7972089	0.94[EUR][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	nsv1044587	chr12:10029514-10123414	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523050	chr12:10031880-10124373	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv898755	chr12:10069302-10186284	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 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	chr12:10078400-10080000	Enhancers	NHEK	skin
2	chr12:10078400-10081000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr12:10078600-10080200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr12:10078600-10080600	Weak transcription	Primary hematopoietic stem cells	blood
5	chr12:10078600-10080800	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr12:10078600-10082600	Weak transcription	NHDF-Ad	bronchial
7	chr12:10078600-10086400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr12:10078600-10086600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:10079000-10081000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr12:10079600-10080000	Enhancers	HUVEC	blood vessel

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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