Variant report

Variant	rs6036732
Chromosome Location	chr20:24297500-24297501
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs6036708	1.00[AMR][1000 genomes]
rs6036716	1.00[AMR][1000 genomes]
rs6036724	1.00[AMR][1000 genomes]
rs6049551	1.00[AMR][1000 genomes]
rs6049552	1.00[AMR][1000 genomes]
rs6049575	0.80[AFR][1000 genomes]
rs6049580	1.00[AMR][1000 genomes]
rs6106809	1.00[AMR][1000 genomes]
rs6114583	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	nsv9793	chr20:23939613-24734850	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv833945	chr20:24163437-24349462	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1058146	chr20:24210196-24531087	Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24297000-24299800	Enhancers	Primary hematopoietic stem cells	blood
2	chr20:24297000-24299800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr20:24297000-24299800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr20:24297000-24300400	Enhancers	Primary T cells from cord blood	blood
5	chr20:24297200-24298400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr20:24297400-24297800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr20:24297400-24298000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr20:24297400-24299800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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