Variant report

Variant	rs74060314
Chromosome Location	chr12:10441924-10441925
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs12581396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60361310	1.00[AMR][1000 genomes]
rs60414299	1.00[AMR][1000 genomes]
rs74060313	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74060317	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74060322	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74060329	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74060337	1.00[AMR][1000 genomes]
rs74062123	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062130	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062131	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062136	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062142	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062144	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062150	0.86[AFR][1000 genomes]
rs74062152	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062159	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062160	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74062163	1.00[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	nsv898757	chr12:10229281-10614641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv832328	chr12:10398071-10620443	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10429000-10442000	Weak transcription	Left Ventricle	heart
2	chr12:10438800-10443600	Weak transcription	Primary T cells from cord blood	blood
3	chr12:10441400-10442000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:10441600-10442000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
5	chr12:10441800-10442200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr12:10441800-10442600	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr12:10441800-10445200	Weak transcription	Primary T helper naive 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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