Variant report

Variant	rs6714724
Chromosome Location	chr2:74113155-74113156
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11890369	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11892479	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11897051	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs12105840	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13414927	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs13418993	0.90[EUR][1000 genomes]
rs13419314	0.90[EUR][1000 genomes]
rs13432600	0.90[EUR][1000 genomes]
rs3738845	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs3813233	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3813234	0.91[ASN][1000 genomes]
rs56875063	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59974236	0.85[ASN][1000 genomes]
rs60987687	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs61314551	0.85[ASN][1000 genomes]
rs6705766	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6744169	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6747730	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6756768	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72917409	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72917413	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72917415	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72917417	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72917422	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72917443	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72917445	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72917450	0.91[ASN][1000 genomes]
rs73948041	0.91[ASN][1000 genomes]
rs7565869	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7579755	0.90[EUR][1000 genomes]
rs7581248	1.00[CHB][hapmap];0.85[ASN][1000 genomes]
rs7600291	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs7600452	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7607601	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:74097600-74114600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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