Variant report

Variant	rs16969353
Chromosome Location	chr15:33616594-33616595
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10519811	0.82[CHB][hapmap]
rs10519812	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs11636989	1.00[CEU][hapmap]
rs11639392	0.97[EUR][1000 genomes]
rs16969005	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs16969361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16969847	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs16969851	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs16969998	0.88[JPT][hapmap]
rs2879378	0.90[EUR][1000 genomes]
rs3907986	1.00[CEU][hapmap]

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	nsv482299	chr15:33449137-33624122	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv533346	chr15:33469439-33809641	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv832963	chr15:33514798-33712442	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv832964	chr15:33608771-33784018	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33614400-33617000	Enhancers	Fetal Thymus	thymus
2	chr15:33615600-33616800	Enhancers	GM12878-XiMat	blood
3	chr15:33615600-33617200	Enhancers	Primary B cells from peripheral blood	blood
4	chr15:33616000-33616600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr15:33616200-33620400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:33616200-33620800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:33616400-33617400	Weak transcription	Thymus	Thymus

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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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