Variant report

Variant	rs7763286
Chromosome Location	chr6:118428100-118428101
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11964013	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11964063	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11967448	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1334829	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1334835	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1334837	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2011710	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs205960	1.00[EUR][1000 genomes]
rs205964	0.82[EUR][1000 genomes]
rs205969	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs205970	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs205973	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs205974	1.00[EUR][1000 genomes]
rs2105019	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2484142	1.00[ASN][1000 genomes]
rs2484144	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2484148	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2484149	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2501517	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28706497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2991964	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs451051	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73516320	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73516324	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73516326	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs928597	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs933067	1.00[EUR][1000 genomes];1.00[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	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118424000-118430600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:118425400-118430400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:118428000-118428400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:118428000-118436200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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