Variant report

Variant	rs9927579
Chromosome Location	chr16:80626910-80626911
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10395	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1452501	0.84[CHB][hapmap];0.83[JPT][hapmap]
rs1452502	0.84[CHB][hapmap];0.83[JPT][hapmap]
rs1562989	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1985288	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2316156	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2316157	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4281727	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4516240	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4547350	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4622522	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7202869	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7405439	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8053414	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9923392	0.84[CHB][hapmap];0.83[JPT][hapmap]
rs9923760	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9932574	0.82[EUR][1000 genomes]
rs9936948	0.94[AMR][1000 genomes];0.85[EUR][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	nsv1060621	chr16:80532848-80980616	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
2	nsv542989	chr16:80532848-80980616	Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	esv3442318	chr16:80626351-80628649	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80619200-80632600	Weak transcription	Hela-S3	cervix
2	chr16:80621200-80628200	Weak transcription	Placenta	Placenta
3	chr16:80625400-80645600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr16:80625600-80636000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr16:80625600-80637800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr16:80626000-80639800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr16:80626200-80637800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr16:80626200-80640000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr16:80626200-80640000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr16:80626400-80636800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr16:80626600-80636600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr16:80626600-80637800	Weak transcription	Liver	Liver
13	chr16:80626800-80645800	Weak transcription	Right Ventricle	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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