Variant report

Variant	rs1149470
Chromosome Location	chr8:64608119-64608120
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10090357	0.81[EUR][1000 genomes]
rs10090496	0.81[EUR][1000 genomes]
rs10106342	0.80[EUR][1000 genomes]
rs10504366	0.84[AFR][1000 genomes]
rs1149456	0.91[EUR][1000 genomes]
rs1149457	0.91[EUR][1000 genomes]
rs1149471	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1149472	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1149473	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1149474	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1149475	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1217096	0.85[EUR][1000 genomes]
rs1217098	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1217099	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1217101	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1217103	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1217106	0.87[EUR][1000 genomes]
rs1217107	0.99[EUR][1000 genomes]
rs1217108	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1217109	0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1217110	0.97[EUR][1000 genomes]
rs1238050	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16930633	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16930637	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17215671	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28439112	0.82[EUR][1000 genomes]
rs28542151	0.83[EUR][1000 genomes]
rs28549862	0.83[EUR][1000 genomes]
rs28721440	0.83[EUR][1000 genomes]
rs57093124	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66503419	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66513944	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66707855	0.80[EUR][1000 genomes]
rs67344323	0.85[EUR][1000 genomes]
rs67801322	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6980548	0.80[EUR][1000 genomes]
rs6992714	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72649240	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs751769	0.92[EUR][1000 genomes]
rs7813066	0.85[ASN][1000 genomes]
rs7824991	0.80[EUR][1000 genomes]
rs7834364	0.81[EUR][1000 genomes]
rs790563	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs790564	0.87[EUR][1000 genomes]
rs790565	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs790566	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs790567	0.85[EUR][1000 genomes]
rs790569	0.81[EUR][1000 genomes]
rs790571	0.92[EUR][1000 genomes]
rs806255	0.85[EUR][1000 genomes]
rs966294	0.89[EUR][1000 genomes]
rs978336	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831343	chr8:64436268-64642328	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:64601400-64614000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:64601800-64615200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr8:64602000-64614800	Weak transcription	Fetal Brain Male	brain

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