Variant report

Variant	rs7158564
Chromosome Location	chr14:72834181-72834182
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs2239227	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2239251	0.82[AMR][1000 genomes]
rs55916717	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56326625	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs57360450	0.85[ASN][1000 genomes]
rs60993427	1.00[ASN][1000 genomes]
rs6574066	0.84[AMR][1000 genomes]
rs72721902	0.87[AMR][1000 genomes]
rs72724044	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs72724054	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs72724074	0.85[ASN][1000 genomes]
rs72724081	0.91[ASN][1000 genomes]
rs72724092	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs72724098	0.87[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8007684	0.93[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs8008045	0.93[CHB][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs8018927	0.84[AMR][1000 genomes]
rs8022845	0.93[CHB][hapmap];0.92[JPT][hapmap];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72829600-72834400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr14:72833200-72834600	Strong transcription	Cortex derived primary cultured neurospheres	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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