Variant report

Variant	rs1391356
Chromosome Location	chr3:111260186-111260187
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10511298	1.00[ASW][hapmap];0.92[CEU][hapmap];0.91[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.86[MEX][hapmap];0.83[MKK][hapmap];0.87[YRI][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10934101	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11916952	0.92[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1391358	0.87[ASN][1000 genomes]
rs1497990	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1513323	1.00[JPT][hapmap]
rs1603687	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2088468	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2276873	0.96[CEU][hapmap];0.89[GIH][hapmap];0.90[TSI][hapmap];0.95[EUR][1000 genomes]
rs2399391	0.93[AFR][1000 genomes]
rs6764960	1.00[JPT][hapmap];0.92[YRI][hapmap];0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6788797	1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs721336	0.95[JPT][hapmap]
rs7616420	1.00[ASW][hapmap];0.92[CEU][hapmap];0.91[CHB][hapmap];0.84[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];0.81[MEX][hapmap];0.90[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7619086	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7628253	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7653347	0.96[CEU][hapmap];0.89[GIH][hapmap];0.90[TSI][hapmap];0.95[EUR][1000 genomes]
rs883113	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs924262	1.00[CEU][hapmap];0.91[CHB][hapmap];0.84[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.90[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs968910	0.86[JPT][hapmap]
rs9855343	0.86[ASN][1000 genomes]

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	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv997756	chr3:111226058-111376585	Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv3946	chr3:111236035-111283038	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1391356	SLC35A5	cis	cerebellum	SCAN

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111255800-111264400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr3:111257200-111261000	Enhancers	Primary B cells from peripheral blood	blood
3	chr3:111258000-111260200	Weak transcription	Small Intestine	intestine
4	chr3:111258000-111261200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr3:111258600-111260600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr3:111258600-111260600	Enhancers	Fetal Thymus	thymus
7	chr3:111258600-111260800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr3:111258600-111265200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:111258600-111266800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr3:111258800-111260200	Weak transcription	Primary hematopoietic stem cells	blood
11	chr3:111258800-111260200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr3:111258800-111260200	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr3:111258800-111260200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:111258800-111260400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:111258800-111260400	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr3:111258800-111260400	Enhancers	Primary T helper cells fromperipheralblood	blood
17	chr3:111258800-111260400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr3:111258800-111260400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr3:111258800-111260400	Weak transcription	Fetal Lung	lung
20	chr3:111258800-111260800	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr3:111258800-111260800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr3:111258800-111261000	Weak transcription	Rectal Mucosa Donor 29	rectum
23	chr3:111258800-111264200	Weak transcription	Stomach Mucosa	stomach
24	chr3:111258800-111266600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr3:111259000-111260200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr3:111259000-111260200	Enhancers	Dnd41	blood
27	chr3:111259000-111260800	Weak transcription	Duodenum Mucosa	Duodenum
28	chr3:111259000-111264000	Weak transcription	Fetal Intestine Small	intestine
29	chr3:111259200-111260200	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr3:111259200-111260600	Weak transcription	Primary B cells from cord blood	blood
31	chr3:111259400-111260400	Enhancers	Primary T cells from cord blood	blood
32	chr3:111259600-111260400	Weak transcription	Thymus	Thymus
33	chr3:111259800-111260200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr3:111259800-111260600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:111260000-111260400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
36	chr3:111260000-111260800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr3:111260000-111261000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr3:111260000-111261000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr3:111260000-111261200	Enhancers	NH-A	brain

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