Variant report

Variant	rs516344
Chromosome Location	chr11:83261682-83261683
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10792688	0.82[CHB][hapmap]
rs10898134	0.85[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11233663	0.82[CEU][hapmap];0.85[CHB][hapmap];0.85[ASN][1000 genomes]
rs11233667	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1367984	0.83[CHB][hapmap]
rs1367985	0.82[CHB][hapmap]
rs1367987	0.85[CHB][hapmap]
rs1432052	0.83[CHB][hapmap]
rs1432057	0.85[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1432058	0.83[CHB][hapmap]
rs1465668	0.85[ASN][1000 genomes]
rs1465671	0.82[CHB][hapmap]
rs2116483	0.82[CHB][hapmap]
rs2195801	0.82[CHB][hapmap]
rs2436156	0.92[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs3793945	0.81[CEU][hapmap];0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs3793946	0.86[CHB][hapmap]
rs3815988	0.82[CHB][hapmap]
rs4316529	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4399351	0.83[CHB][hapmap]
rs4494323	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4547114	0.83[CHB][hapmap]
rs472415	0.87[CHB][hapmap]
rs485199	0.85[CEU][hapmap]
rs489567	0.84[CEU][hapmap]
rs494303	0.92[CEU][hapmap]
rs500571	0.81[CHB][hapmap]
rs515618	0.92[CEU][hapmap]
rs516435	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];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs532467	0.96[CEU][hapmap]
rs535755	0.81[EUR][1000 genomes]
rs541133	0.92[CEU][hapmap];0.83[CHB][hapmap];0.83[EUR][1000 genomes]
rs543068	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs546557	0.92[CEU][hapmap];0.90[CHB][hapmap];0.83[EUR][1000 genomes]
rs548327	0.96[CEU][hapmap];0.81[EUR][1000 genomes]
rs551108	0.85[CEU][hapmap]
rs558211	0.92[CEU][hapmap]
rs560846	0.81[EUR][1000 genomes]
rs561890	0.96[CEU][hapmap];0.90[CHB][hapmap]
rs571331	0.92[CEU][hapmap];0.83[CHB][hapmap];0.83[EUR][1000 genomes]
rs574361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs591422	0.92[CEU][hapmap]
rs61902066	0.84[EUR][1000 genomes]
rs635823	0.88[CEU][hapmap]
rs645427	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs651491	0.81[CEU][hapmap]
rs653546	0.88[CEU][hapmap]
rs656727	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs658438	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6592120	0.81[CHB][hapmap];0.80[JPT][hapmap];0.81[ASN][1000 genomes]
rs6592123	0.82[CHB][hapmap]
rs6592124	0.83[CHB][hapmap]
rs6592125	0.89[ASN][1000 genomes]
rs659427	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs666845	0.81[CHB][hapmap]
rs671313	0.92[CEU][hapmap];0.82[CHB][hapmap];0.83[EUR][1000 genomes]
rs676115	0.96[CEU][hapmap]
rs684857	0.81[CHB][hapmap]
rs688997	0.85[CEU][hapmap]
rs694847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7113167	0.86[CHB][hapmap];0.80[JPT][hapmap];0.85[ASN][1000 genomes]
rs7924348	0.85[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7926588	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];0.99[ASN][1000 genomes]
rs7927435	0.85[ASN][1000 genomes]
rs7928931	0.81[CEU][hapmap];0.86[CHB][hapmap];0.91[ASN][1000 genomes]
rs7930252	0.83[CHB][hapmap]
rs7939707	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7940037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83257200-83265600	Weak transcription	Fetal Stomach	stomach
2	chr11:83258200-83261800	Weak transcription	Brain Substantia Nigra	brain
3	chr11:83259200-83261800	Enhancers	Hela-S3	cervix
4	chr11:83260000-83262600	Enhancers	Brain Cingulate Gyrus	brain
5	chr11:83260200-83262400	Enhancers	Brain Hippocampus Middle	brain
6	chr11:83261000-83261800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr11:83261000-83262800	Enhancers	Brain Angular Gyrus	brain
8	chr11:83261200-83261800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr11:83261200-83261800	Enhancers	Brain Germinal Matrix	brain
10	chr11:83261400-83261800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:83261400-83262000	Enhancers	NHEK	skin
12	chr11:83261400-83262600	Enhancers	Fetal Heart	heart
13	chr11:83261600-83261800	Enhancers	Fetal Lung	lung
14	chr11:83261600-83263200	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr11:83261600-83266000	Weak transcription	Brain Anterior Caudate	brain

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