Variant report

Variant	rs2271492
Chromosome Location	chr3:113302493-113302494
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11929640	0.83[GIH][hapmap];0.87[TSI][hapmap]
rs12631929	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1567779	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1567781	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2048624	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2271493	0.93[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[YRI][hapmap];0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2271495	1.00[CHB][hapmap];0.98[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2292510	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2292511	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28446408	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28530478	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28564696	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34842926	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3773691	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3821682	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3821683	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3896909	1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3932276	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs41271363	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4560271	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4560272	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4682493	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4682494	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4682496	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.90[TSI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4682497	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55941419	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56721892	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62265514	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62265515	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62265518	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62265520	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62265521	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6787428	0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72950888	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7637206	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9816095	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9823358	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9844542	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9854140	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9863703	0.87[GIH][hapmap];0.84[MEX][hapmap];0.83[MKK][hapmap];0.96[TSI][hapmap]
rs9868243	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9874993	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9879239	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9985452	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[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	nsv1013506	chr3:112890608-113680951	Weak transcription Bivalent/Poised TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv1004000	chr3:113116778-113513899	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv877349	chr3:113208224-113323787	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
4	nsv877350	chr3:113208224-113332235	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs2271492	SIDT1	cis	cerebellum	SCAN
rs2271492	SIDT1	cis	parietal	SCAN

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113280200-113321600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:113280400-113304000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:113280600-113314800	Weak transcription	Spleen	Spleen
4	chr3:113285200-113329800	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:113285200-113343400	Weak transcription	Small Intestine	intestine
6	chr3:113286000-113316800	Weak transcription	Brain Angular Gyrus	brain
7	chr3:113294400-113321600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr3:113294800-113304200	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr3:113296800-113303600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr3:113296800-113324200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
11	chr3:113297400-113315600	Strong transcription	GM12878-XiMat	blood
12	chr3:113297800-113308000	Strong transcription	Primary T cells from cord blood	blood
13	chr3:113298800-113309400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr3:113298800-113315200	Strong transcription	Primary B cells from peripheral blood	blood
15	chr3:113299400-113302600	Strong transcription	Rectal Mucosa Donor 29	rectum
16	chr3:113299400-113308000	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr3:113299400-113315400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr3:113299600-113306400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr3:113299600-113309400	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr3:113299800-113303600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr3:113300000-113302600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
22	chr3:113300400-113302800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr3:113300800-113303400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr3:113300800-113308800	Weak transcription	Thymus	Thymus
25	chr3:113301800-113302600	Weak transcription	Fetal Thymus	thymus
26	chr3:113301800-113302800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr3:113302000-113308200	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr3:113302200-113305400	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr3:113302200-113308400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr3:113302200-113309400	Strong transcription	Primary B cells from cord blood	blood
31	chr3:113302400-113303000	Enhancers	HepG2	liver
32	chr3:113302400-113304600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr3:113302400-113306000	Strong transcription	Primary T killer memory cells from peripheral blood	blood

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