Variant report

Variant	rs73054969
Chromosome Location	chr2:205893210-205893211
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10084396	1.00[EUR][1000 genomes]
rs10166926	1.00[EUR][1000 genomes]
rs1510766	1.00[EUR][1000 genomes]
rs1567502	1.00[EUR][1000 genomes]
rs4145000	1.00[EUR][1000 genomes]
rs4673312	1.00[EUR][1000 genomes]
rs4675479	1.00[EUR][1000 genomes]
rs4675480	1.00[EUR][1000 genomes]
rs4675483	1.00[EUR][1000 genomes]
rs6748535	1.00[EUR][1000 genomes]
rs73054972	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73054975	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs73982803	1.00[EUR][1000 genomes]
rs7580880	1.00[EUR][1000 genomes]
rs976118	1.00[EUR][1000 genomes]
rs976119	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998485	chr2:205407813-206184006	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv536122	chr2:205407813-206184006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1010210	chr2:205489653-206076013	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv875728	chr2:205853136-205906945	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205878600-205895400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:205887800-205906200	Weak transcription	Pancreas	Pancrea
3	chr2:205890600-205894000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr2:205890800-205895600	Weak transcription	HSMMtube	muscle
5	chr2:205890800-205897400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr2:205890800-205898800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr2:205890800-205899600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:205891000-205901000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:205891400-205893800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr2:205891600-205893600	Weak transcription	Primary T cells from cord blood	blood
11	chr2:205891600-205897600	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr2:205891800-205894400	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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