Variant report

Variant	rs73264056
Chromosome Location	chr12:22320066-22320067
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs36064966	0.80[AFR][1000 genomes]
rs61323744	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66529819	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs67115831	0.85[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs71448638	0.98[ASN][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	esv2758298	chr12:22140834-22339299	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2759883	chr12:22140834-22736907	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 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	chr12:22318000-22322200	Weak transcription	Fetal Thymus	thymus
2	chr12:22318200-22322200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr12:22318200-22322400	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr12:22318400-22322000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr12:22318400-22322200	Weak transcription	Primary B cells from peripheral blood	blood
6	chr12:22318400-22322200	Weak transcription	Primary T helper cells PMA-I stimulated	--
7	chr12:22318800-22321800	Weak transcription	Primary T cells from cord blood	blood

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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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