Variant report

Variant	rs7815202
Chromosome Location	chr8:59096670-59096671
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10086720	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10100258	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10108890	0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10808688	0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10808689	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10957034	0.80[EUR][1000 genomes]
rs11782856	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13251766	0.91[ASN][1000 genomes]
rs13251779	0.86[ASN][1000 genomes]
rs13260332	0.95[EUR][1000 genomes]
rs13261171	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13262713	0.93[EUR][1000 genomes]
rs13275097	0.81[ASN][1000 genomes]
rs1507084	0.81[ASN][1000 genomes]
rs1876379	0.92[EUR][1000 genomes]
rs2048103	0.91[EUR][1000 genomes]
rs2221576	0.93[EUR][1000 genomes]
rs28621890	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2939974	0.87[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2977384	0.96[ASN][1000 genomes]
rs2977386	0.99[ASN][1000 genomes]
rs2977390	0.94[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2977391	0.94[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs34415132	0.81[ASN][1000 genomes]
rs35320500	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35764763	0.96[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36094668	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4373508	0.97[ASN][1000 genomes]
rs4398899	0.97[ASN][1000 genomes]
rs7464538	0.88[EUR][1000 genomes]
rs7833271	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs979444	0.80[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:59084200-59099800	Weak transcription	Fetal Brain Female	brain
2	chr8:59093200-59103200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:59093400-59097600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:59093400-59105600	Weak transcription	HMEC	breast
5	chr8:59095800-59096800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr8:59096400-59097200	Enhancers	Primary monocytes fromperipheralblood	blood

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