Variant report

Variant	rs12977631
Chromosome Location	chr19:39242461-39242462
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs11083478	0.96[ASN][1000 genomes]
rs12972997	1.00[ASN][1000 genomes]
rs12979149	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12980798	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12985030	1.00[ASN][1000 genomes]
rs2086147	0.89[ASN][1000 genomes]
rs2100941	0.96[ASN][1000 genomes]
rs2368524	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34054765	1.00[ASN][1000 genomes]
rs34090445	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34305426	1.00[ASN][1000 genomes]
rs34361849	0.81[ASN][1000 genomes]
rs34776027	0.96[ASN][1000 genomes]
rs34834035	0.96[ASN][1000 genomes]
rs35026669	0.93[ASN][1000 genomes]
rs35253157	0.87[ASN][1000 genomes]
rs35335944	0.96[ASN][1000 genomes]
rs35502825	0.96[ASN][1000 genomes]
rs35604174	0.96[ASN][1000 genomes]
rs35974114	0.93[ASN][1000 genomes]
rs4435378	0.96[ASN][1000 genomes]
rs4473308	0.96[ASN][1000 genomes]
rs4474812	0.96[ASN][1000 genomes]
rs4491650	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4801868	0.96[ASN][1000 genomes]
rs4802795	0.96[ASN][1000 genomes]
rs4802796	0.96[ASN][1000 genomes]
rs56817884	1.00[ASN][1000 genomes]
rs58794115	0.85[ASN][1000 genomes]
rs59073128	0.96[ASN][1000 genomes]
rs61121905	1.00[ASN][1000 genomes]
rs61417362	0.93[ASN][1000 genomes]
rs62120085	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62120091	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62120094	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62120159	1.00[ASN][1000 genomes]
rs62121364	0.82[AMR][1000 genomes]
rs62121365	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62121373	0.96[ASN][1000 genomes]
rs62121374	0.96[ASN][1000 genomes]
rs62121375	0.96[ASN][1000 genomes]
rs7253700	0.96[ASN][1000 genomes]
rs7257060	0.89[ASN][1000 genomes]
rs7257063	0.89[ASN][1000 genomes]
rs73554745	0.96[ASN][1000 genomes]
rs7508528	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833828	chr19:39084759-39257979	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1057899	chr19:39088319-39475493	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv911668	chr19:39174669-39291771	Genic enhancers Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	esv1826260	chr19:39178364-39248836	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
5	esv1837023	chr19:39190588-39425722	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 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	chr19:39235200-39244400	Weak transcription	HepG2	liver
2	chr19:39236600-39245600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:39241200-39244400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:39241600-39244200	Weak transcription	K562	blood

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