Variant report

Variant	rs1500878
Chromosome Location	chr3:112576258-112576259
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10934190	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10934192	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10934193	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13326243	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1500879	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1971986	0.80[AMR][1000 genomes]
rs2101440	0.81[AMR][1000 genomes]
rs2399436	0.80[AMR][1000 genomes]
rs28859668	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs28867393	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4234417	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4478054	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4571210	0.94[ASN][1000 genomes]
rs4682120	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4682444	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6438111	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6438112	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6438113	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6438114	0.97[ASN][1000 genomes]
rs6763318	0.81[CHB][hapmap];0.90[JPT][hapmap]
rs6765379	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6791158	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6791672	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7632218	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7651207	0.81[JPT][hapmap]
rs9814008	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs9818564	0.97[ASN][1000 genomes]
rs9834599	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs9838082	0.87[ASN][1000 genomes]
rs9868839	0.81[AMR][1000 genomes]
rs9875551	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9879005	0.90[CHB][hapmap];0.90[JPT][hapmap]
rs9879149	0.95[CHB][hapmap];0.84[JPT][hapmap]

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	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv432477	chr3:112390310-112603310	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3431441	chr3:112453467-113213252	Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
4	nsv877343	chr3:112470586-112597706	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv3501334	chr3:112546820-112648766	Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv3501335	chr3:112546820-112648766	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112574400-112578200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr3:112574600-112578600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr3:112574800-112576800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr3:112574800-112577600	Enhancers	Primary T helper naive cells from peripheral blood	blood
5	chr3:112574800-112578400	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr3:112575000-112576800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr3:112575000-112577800	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr3:112575000-112578000	Enhancers	Primary B cells from peripheral blood	blood
9	chr3:112575200-112576400	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr3:112575200-112576800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr3:112575200-112577800	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr3:112575200-112578200	Enhancers	Primary B cells from cord blood	blood
13	chr3:112575200-112578800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr3:112575800-112578000	ZNF genes & repeats	GM12878-XiMat	blood
15	chr3:112576000-112576400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:112576000-112576800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr3:112576000-112577200	Weak transcription	Primary T cells fromperipheralblood	blood
18	chr3:112576000-112577200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr3:112576000-112577400	Weak transcription	K562	blood
20	chr3:112576200-112576800	Weak transcription	Primary T helper cells PMA-I stimulated	--

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