Variant report

Variant	rs12331776
Chromosome Location	chr4:120617412-120617413
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10001829	0.81[EUR][1000 genomes]
rs10005075	0.81[EUR][1000 genomes]
rs10005177	0.81[EUR][1000 genomes]
rs10007283	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10011345	0.82[EUR][1000 genomes]
rs10011928	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10014793	0.82[EUR][1000 genomes]
rs10018153	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10023652	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10023655	0.81[EUR][1000 genomes]
rs10029669	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12502919	0.83[EUR][1000 genomes]
rs12510467	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12512171	0.81[EUR][1000 genomes]
rs13103043	0.81[EUR][1000 genomes]
rs13112498	0.81[EUR][1000 genomes]
rs13119146	0.81[EUR][1000 genomes]
rs13141413	0.81[EUR][1000 genomes]
rs13328038	0.81[EUR][1000 genomes]
rs17005485	0.82[EUR][1000 genomes]
rs17005677	0.81[EUR][1000 genomes]
rs2256834	0.80[EUR][1000 genomes]
rs2389900	0.84[EUR][1000 genomes]
rs2389903	0.82[EUR][1000 genomes]
rs2389904	0.82[EUR][1000 genomes]
rs2714972	0.80[EUR][1000 genomes]
rs28642385	0.84[EUR][1000 genomes]
rs28663988	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs28706824	0.81[EUR][1000 genomes]
rs28723049	0.80[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28847617	0.80[EUR][1000 genomes]
rs28869613	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4001169	0.82[EUR][1000 genomes]
rs4094	0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4337717	0.82[EUR][1000 genomes]
rs4833625	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4834802	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4834805	0.84[EUR][1000 genomes]
rs4834808	0.81[EUR][1000 genomes]
rs749525	0.81[EUR][1000 genomes]
rs749526	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7655035	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7669436	0.82[EUR][1000 genomes]
rs7683474	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7693769	0.81[EUR][1000 genomes]
rs7699252	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs874425	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9998665	0.81[EUR][1000 genomes]
rs9999212	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv532739	chr4:120392824-121098103	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
3	nsv1010753	chr4:120429028-120684310	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537233	chr4:120429028-120684310	ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1006572	chr4:120432494-120694243	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1802546	chr4:120558608-120675026	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1010638	chr4:120586178-120671835	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1009771	chr4:120590902-120665812	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs12331776	FLJ14186///LOC284701///LOC441124///LOC728624	Cis_chr	lymphoblastoid	RTeQTL
rs12331776	LOC645513	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120614400-120619200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:120616400-120617800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:120617400-120617600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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