Variant report

Variant	rs11031729
Chromosome Location	chr11:32365066-32365067
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10767930	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10767931	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10835887	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10835888	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10835889	0.93[ASN][1000 genomes]
rs11031724	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11031726	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11031728	0.93[ASN][1000 genomes]
rs11031731	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11031733	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12099181	0.82[AFR][1000 genomes]
rs12278882	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12280757	0.93[ASN][1000 genomes]
rs12789861	0.85[AFR][1000 genomes]
rs17673047	1.00[CHB][hapmap]
rs2057178	1.00[ASN][1000 genomes]
rs2207549	1.00[YRI][hapmap];0.93[AFR][1000 genomes]
rs61889183	0.93[ASN][1000 genomes]
rs61889186	0.96[ASN][1000 genomes]
rs61889187	0.96[ASN][1000 genomes]
rs7106353	0.93[ASN][1000 genomes]
rs7122775	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7123725	0.93[ASN][1000 genomes]
rs7127500	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7924866	0.93[ASN][1000 genomes]

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32361000-32372400	Enhancers	Fetal Heart	heart
2	chr11:32363200-32366000	Weak transcription	Fetal Stomach	stomach
3	chr11:32363400-32365200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr11:32364400-32366400	Enhancers	Dnd41	blood
5	chr11:32364800-32365600	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr11:32364800-32365800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:32364800-32365800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:32365000-32365400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
9	chr11:32365000-32365600	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr11:32365000-32365600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr11:32365000-32365600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr11:32365000-32365600	Enhancers	GM12878-XiMat	blood
13	chr11:32365000-32365800	Enhancers	Primary T cells from cord blood	blood
14	chr11:32365000-32365800	Enhancers	Primary hematopoietic stem cells	blood
15	chr11:32365000-32365800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr11:32365000-32365800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr11:32365000-32366200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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