Variant report

Variant	rs11031728
Chromosome Location	chr11:32363616-32363617
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10767930	0.96[ASN][1000 genomes]
rs10767931	0.96[ASN][1000 genomes]
rs10835887	1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs10835888	0.81[CEU][hapmap];1.00[CHB][hapmap];0.93[ASN][1000 genomes]
rs10835889	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11031714	0.88[EUR][1000 genomes]
rs11031716	0.92[EUR][1000 genomes]
rs11031724	1.00[ASN][1000 genomes]
rs11031726	0.96[ASN][1000 genomes]
rs11031729	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11031731	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11031733	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11828433	0.92[EUR][1000 genomes]
rs12278882	1.00[ASN][1000 genomes]
rs12280757	1.00[ASN][1000 genomes]
rs12285028	0.91[EUR][1000 genomes]
rs12285041	0.91[EUR][1000 genomes]
rs17673047	1.00[CHB][hapmap]
rs2057178	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61889170	0.86[EUR][1000 genomes]
rs61889172	0.86[EUR][1000 genomes]
rs61889173	0.86[EUR][1000 genomes]
rs61889183	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61889186	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61889187	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7106353	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7121219	0.88[EUR][1000 genomes]
rs7122775	0.89[ASN][1000 genomes]
rs7123725	1.00[ASN][1000 genomes]
rs7127500	1.00[ASN][1000 genomes]
rs7924866	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32356800-32364400	Weak transcription	Dnd41	blood
2	chr11:32361000-32372400	Enhancers	Fetal Heart	heart
3	chr11:32363200-32366000	Weak transcription	Fetal Stomach	stomach
4	chr11:32363400-32363800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr11:32363400-32364400	Weak transcription	Fetal Lung	lung
6	chr11:32363400-32365200	Weak transcription	Rectal Smooth Muscle	rectum
7	chr11:32363600-32364800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links