Variant report

Variant	rs62521231
Chromosome Location	chr8:118572543-118572544
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10505295	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10505315	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11997337	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1396347	0.81[ASN][1000 genomes]
rs16889833	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16889836	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16889862	0.91[ASN][1000 genomes]
rs17667915	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17668076	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17668088	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17740505	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17746363	0.81[ASN][1000 genomes]
rs17746428	0.81[ASN][1000 genomes]
rs28571816	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3937768	0.92[ASN][1000 genomes]
rs62521183	0.81[EUR][1000 genomes]
rs62521198	0.84[EUR][1000 genomes]
rs62521200	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62521203	0.91[ASN][1000 genomes]
rs62521228	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62521229	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62521240	0.83[ASN][1000 genomes]
rs62521243	0.81[ASN][1000 genomes]
rs62521245	0.83[ASN][1000 genomes]
rs717349	0.86[ASN][1000 genomes]
rs737298	0.83[ASN][1000 genomes]
rs749492	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs755982	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs922587	0.94[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118564600-118573200	Weak transcription	Aorta	Aorta
2	chr8:118572000-118572800	Enhancers	Primary B cells from peripheral blood	blood
3	chr8:118572000-118573000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr8:118572000-118573000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr8:118572200-118572600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:118572200-118572600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:118572200-118572800	Enhancers	Dnd41	blood
8	chr8:118572400-118572800	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr8:118572400-118572800	Enhancers	Spleen	Spleen

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