Variant report

Variant	rs72988047
Chromosome Location	chr6:55469291-55469292
allele	A/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:27)

rs_ID	r²[population]
rs11752812	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11753028	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11753553	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11754509	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11756219	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11756598	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11758071	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11759233	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11961322	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13195454	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs228152	1.00[ASN][1000 genomes]
rs6923399	1.00[ASN][1000 genomes]
rs72874012	1.00[ASN][1000 genomes]
rs72874020	1.00[ASN][1000 genomes]
rs72874021	1.00[ASN][1000 genomes]
rs72973115	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72973134	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72973139	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72973142	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72973143	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72975079	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72975085	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72975086	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72975090	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72975095	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72976261	1.00[ASN][1000 genomes]
rs72988067	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv948358	chr6:55351282-55477277	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1026411	chr6:55372845-55653498	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	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	chr6:55463600-55474600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:55466200-55473600	Weak transcription	Pancreas	Pancrea
3	chr6:55468800-55472600	Weak transcription	Fetal Lung	lung

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