Variant report

Variant	rs60076255
Chromosome Location	chr15:55108106-55108107
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11634525	0.89[AFR][1000 genomes]
rs13380345	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1566566	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1909944	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56909278	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60820899	0.96[AFR][1000 genomes]
rs73411776	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73411787	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73411799	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73413703	0.89[AFR][1000 genomes]
rs73413706	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73413710	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73413714	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73413739	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73413743	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73413745	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73413750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs988653	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833013	chr15:54927825-55135274	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv1035785	chr15:54951691-55266222	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv542390	chr15:54951691-55266222	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1039860	chr15:55010228-55198111	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1043176	chr15:55010228-55563000	Genic enhancers Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	nsv1042741	chr15:55068022-55622497	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
7	nsv525041	chr15:55068209-55136755	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv977070	chr15:55096487-55120028	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv1047424	chr15:55098585-55243518	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv833014	chr15:55099183-55249491	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55107200-55108800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr15:55107200-55109000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr15:55107200-55109000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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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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