Variant report

Variant	rs10946615
Chromosome Location	chr6:23672844-23672845
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10456277	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10456278	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10456279	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10946617	0.85[EUR][1000 genomes]
rs11964821	0.83[EUR][1000 genomes]
rs12191024	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12191124	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12191169	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12198734	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12198796	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12205517	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12207724	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs12209291	0.85[EUR][1000 genomes]
rs12210770	0.84[EUR][1000 genomes]
rs12212370	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12212408	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12212513	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12214844	0.86[EUR][1000 genomes]
rs13202207	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13216480	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs34217675	0.86[EUR][1000 genomes]
rs34444313	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34911525	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35466548	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35750020	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35776872	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6456565	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6900150	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6921301	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6929007	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6931060	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv462656	chr6:23629281-23721032	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
3	nsv601125	chr6:23629281-23721032	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv1027773	chr6:23644898-23776497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:23671400-23674200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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