Variant report

Variant	rs11991231
Chromosome Location	chr8:19907912-19907913
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1011685	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1059611	0.84[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes]
rs11570891	0.85[CEU][hapmap];0.91[JPT][hapmap];0.83[EUR][1000 genomes]
rs11989309	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12678603	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12678604	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12678919	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12679834	0.92[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17411024	0.87[EUR][1000 genomes]
rs17411113	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17482753	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1803924	0.83[EUR][1000 genomes]
rs28675909	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs325	0.92[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs328	0.92[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3735964	0.84[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs4128744	0.91[ASN][1000 genomes]
rs6586884	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6983430	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6999813	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7004149	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7004158	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7007609	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7007797	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7016880	0.96[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9644568	1.00[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][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	nsv610759	chr8:19561997-20068842	Enhancers Strong transcription Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv530877	chr8:19873053-20593254	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv890633	chr8:19875100-19985382	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island 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	chr8:19906800-19911600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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