Variant report

Variant	rs1414283
Chromosome Location	chr6:79979927-79979928
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10455359	1.00[EUR][1000 genomes]
rs10806163	0.86[EUR][1000 genomes]
rs11965180	0.97[EUR][1000 genomes]
rs11966786	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11969279	0.97[EUR][1000 genomes]
rs12194892	0.86[EUR][1000 genomes]
rs12209677	0.86[EUR][1000 genomes]
rs1335535	1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1335537	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1335538	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1414279	0.86[EUR][1000 genomes]
rs1414284	1.00[EUR][1000 genomes]
rs1537739	0.97[EUR][1000 genomes]
rs1537740	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs1582079	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16890450	0.86[EUR][1000 genomes]
rs1832088	1.00[EUR][1000 genomes]
rs1832089	1.00[EUR][1000 genomes]
rs1889685	0.97[EUR][1000 genomes]
rs2095633	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2322216	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2322219	0.97[EUR][1000 genomes]
rs2874732	1.00[EUR][1000 genomes]
rs2874733	1.00[EUR][1000 genomes]
rs3934335	1.00[EUR][1000 genomes]
rs4112504	1.00[EUR][1000 genomes]
rs4235810	0.97[EUR][1000 genomes]
rs4301272	0.97[EUR][1000 genomes]
rs4377755	1.00[EUR][1000 genomes]
rs4407672	1.00[EUR][1000 genomes]
rs4418150	0.85[CEU][hapmap];0.97[EUR][1000 genomes]
rs4432946	0.97[EUR][1000 genomes]
rs4464749	1.00[EUR][1000 genomes]
rs4470813	1.00[EUR][1000 genomes]
rs4537102	0.97[EUR][1000 genomes]
rs4555887	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs4706754	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[YRI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4706755	1.00[CEU][hapmap];0.85[YRI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4706756	1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4706759	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs4706760	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs4706765	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs4706766	1.00[EUR][1000 genomes]
rs55635444	1.00[EUR][1000 genomes]
rs56183421	0.97[EUR][1000 genomes]
rs56193084	0.86[EUR][1000 genomes]
rs56354335	0.86[EUR][1000 genomes]
rs56955811	0.86[EUR][1000 genomes]
rs57340384	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57608966	0.86[EUR][1000 genomes]
rs59152048	1.00[EUR][1000 genomes]
rs59858042	1.00[EUR][1000 genomes]
rs61227507	1.00[EUR][1000 genomes]
rs61558200	0.86[EUR][1000 genomes]
rs62411290	1.00[EUR][1000 genomes]
rs6454106	1.00[EUR][1000 genomes]
rs6907042	1.00[EUR][1000 genomes]
rs6907264	1.00[CEU][hapmap];0.94[YRI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6913297	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs6917165	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6924790	1.00[EUR][1000 genomes]
rs6929660	0.97[EUR][1000 genomes]
rs6941433	1.00[EUR][1000 genomes]
rs73468020	0.89[EUR][1000 genomes]
rs73468035	0.86[EUR][1000 genomes]
rs73767530	0.86[EUR][1000 genomes]
rs7738508	1.00[EUR][1000 genomes]
rs7739118	0.97[EUR][1000 genomes]
rs7746915	1.00[EUR][1000 genomes]
rs7751974	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7752593	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7757062	0.97[EUR][1000 genomes]
rs7760458	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7760939	0.97[EUR][1000 genomes]
rs7763232	1.00[EUR][1000 genomes]
rs7764517	1.00[EUR][1000 genomes]
rs7770245	1.00[EUR][1000 genomes]
rs7772967	1.00[EUR][1000 genomes]
rs9341761	0.95[YRI][hapmap]
rs9343886	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[YRI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9343890	0.95[EUR][1000 genomes]
rs9350803	1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9352710	1.00[EUR][1000 genomes]
rs9359369	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9361504	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9361511	1.00[EUR][1000 genomes]
rs9443654	1.00[CEU][hapmap];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830706	chr6:79825910-79994878	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1028607	chr6:79853272-80767716	Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79978600-79980400	Enhancers	K562	blood
2	chr6:79978800-79980200	Enhancers	Ovary	ovary
3	chr6:79979000-79980400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:79979200-79980200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:79979400-79980200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:79979400-79980200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr6:79979400-79980200	Enhancers	Stomach Smooth Muscle	stomach
8	chr6:79979600-79980000	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr6:79979600-79980000	Enhancers	Fetal Intestine Small	intestine
10	chr6:79979600-79980200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr6:79979600-79980200	Enhancers	Fetal Heart	heart
12	chr6:79979600-79980200	Enhancers	Fetal Intestine Large	intestine
13	chr6:79979600-79980400	Enhancers	Colon Smooth Muscle	Colon
14	chr6:79979800-79980200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:79979800-79980200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:79979800-79980800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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