Variant report

Variant	rs4895893
Chromosome Location	chr6:131103122-131103123
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11154605	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11154606	0.88[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs11154607	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11751010	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1497890	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1605604	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17059550	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1988279	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4897458	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4897462	0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4897467	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62422290	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62425266	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6914815	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6937163	0.92[ASN][1000 genomes]
rs9492710	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9492712	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533971	chr6:130490694-131172051	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv830806	chr6:130938330-131107137	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv604664	chr6:131004998-131115817	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1025019	chr6:131074711-131116070	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv604665	chr6:131077027-131115817	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv604666	chr6:131078180-131122295	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131099800-131103200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
2	chr6:131099800-131103600	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr6:131099800-131103800	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr6:131100000-131103600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr6:131100200-131103600	Enhancers	Primary T cells fromperipheralblood	blood
6	chr6:131100400-131103600	Enhancers	Primary T cells from cord blood	blood
7	chr6:131100400-131103600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr6:131100600-131103600	Enhancers	Fetal Thymus	thymus
9	chr6:131101200-131103600	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr6:131101400-131105600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr6:131101600-131103400	Enhancers	Thymus	Thymus
12	chr6:131101600-131104000	Weak transcription	Fetal Stomach	stomach
13	chr6:131102200-131103600	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr6:131102400-131103600	Enhancers	Dnd41	blood
15	chr6:131102800-131103400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr6:131102800-131103400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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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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