Variant report

Variant	rs1510929
Chromosome Location	chr8:49330104-49330105
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10108217	0.94[EUR][1000 genomes]
rs1317527	1.00[ASN][1000 genomes]
rs13250982	1.00[ASN][1000 genomes]
rs13273913	1.00[ASN][1000 genomes]
rs1502651	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1510930	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16937035	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16937122	1.00[ASN][1000 genomes]
rs16937172	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17623020	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34098567	1.00[ASN][1000 genomes]
rs34634731	1.00[ASN][1000 genomes]
rs35621163	1.00[ASN][1000 genomes]
rs35687493	1.00[ASN][1000 genomes]
rs36018304	1.00[ASN][1000 genomes]
rs36084713	1.00[ASN][1000 genomes]
rs4546689	1.00[ASN][1000 genomes]
rs4633088	0.94[EUR][1000 genomes]
rs56038738	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57556149	0.94[EUR][1000 genomes]
rs6983842	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6990374	1.00[ASN][1000 genomes]
rs6991400	1.00[ASN][1000 genomes]
rs6992602	1.00[ASN][1000 genomes]
rs6996130	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7002586	1.00[ASN][1000 genomes]
rs7012467	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7012795	1.00[ASN][1000 genomes]
rs7013123	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7013144	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7017418	1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs71511915	1.00[ASN][1000 genomes]
rs73678289	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7813028	1.00[EUR][1000 genomes]
rs7813928	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7815397	1.00[ASN][1000 genomes]
rs7815783	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7819527	1.00[ASN][1000 genomes]
rs7831832	1.00[ASN][1000 genomes]
rs7837292	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[EUR][1000 genomes]
rs7838494	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7843782	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs907177	1.00[ASN][1000 genomes]
rs955820	0.93[ASN][1000 genomes]
rs9643364	1.00[EUR][1000 genomes]
rs9694327	0.96[ASN][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49319800-49332400	Weak transcription	Fetal Kidney	kidney
2	chr8:49328000-49331000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:49329800-49332400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr8:49330000-49330200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr8:49330000-49330200	Enhancers	NHLF	lung
6	chr8:49330000-49330400	Enhancers	NH-A	brain
7	chr8:49330000-49331000	Weak transcription	Left Ventricle	heart
8	chr8:49330000-49331800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:49330000-49333800	Enhancers	HUVEC	blood vessel

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