Variant report

Variant	rs73307197
Chromosome Location	chr8:107448733-107448734
allele	A/G
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:19)

rs_ID	r²[population]
rs60293753	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60554121	1.00[AMR][1000 genomes]
rs61677096	0.81[AFR][1000 genomes]
rs6985468	1.00[AMR][1000 genomes]
rs73305148	1.00[AMR][1000 genomes]
rs73305163	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305167	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305173	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305176	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73305190	1.00[AMR][1000 genomes]
rs73309233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73309246	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73309280	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73309281	1.00[AMR][1000 genomes]
rs73309288	0.81[AFR][1000 genomes]
rs73309292	0.81[AFR][1000 genomes]
rs73311204	0.91[AFR][1000 genomes]
rs73311205	0.91[AFR][1000 genomes]
rs7840485	1.00[AMR][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	nsv533134	chr8:107307812-107670002	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv824701	chr8:107378298-107520063	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv611844	chr8:107440038-107494918	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107444800-107451400	Weak transcription	Aorta	Aorta
2	chr8:107446800-107450200	Enhancers	Primary T cells from cord blood	blood
3	chr8:107447000-107451400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr8:107447200-107449000	Enhancers	Primary hematopoietic stem cells	blood
5	chr8:107447400-107451800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr8:107447400-107452600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr8:107447800-107448800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr8:107447800-107448800	Weak transcription	Fetal Thymus	thymus
9	chr8:107447800-107449000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:107447800-107449000	Enhancers	HUVEC	blood vessel
11	chr8:107448400-107449000	Weak transcription	Primary hematopoietic stem cells short term culture	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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