Variant report

Variant	rs7617799
Chromosome Location	chr3:151217740-151217741
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10935861	0.84[EUR][1000 genomes]
rs11712630	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12630095	0.96[CEU][hapmap];0.90[CHB][hapmap];0.83[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12634284	0.91[EUR][1000 genomes]
rs12639049	0.91[EUR][1000 genomes]
rs13315624	0.92[EUR][1000 genomes]
rs4128734	0.86[EUR][1000 genomes]
rs4345047	0.84[EUR][1000 genomes]
rs4350898	0.90[EUR][1000 genomes]
rs4481136	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4484172	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4608665	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4679836	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap];0.92[EUR][1000 genomes]
rs4679837	0.89[CEU][hapmap];0.84[CHB][hapmap]
rs4680464	0.92[EUR][1000 genomes]
rs4680465	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[JPT][hapmap];0.92[EUR][1000 genomes]
rs4680473	0.94[EUR][1000 genomes]
rs4680501	0.82[EUR][1000 genomes]
rs6440744	0.83[EUR][1000 genomes]
rs6440745	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6440748	0.85[EUR][1000 genomes]
rs6440763	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6798066	0.96[CEU][hapmap];0.86[EUR][1000 genomes]
rs6805953	0.89[EUR][1000 genomes]
rs7375135	0.86[EUR][1000 genomes]
rs7427312	0.85[EUR][1000 genomes]
rs7617486	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7629172	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7629867	0.92[EUR][1000 genomes]
rs7629912	0.90[EUR][1000 genomes]
rs7636304	0.85[EUR][1000 genomes]
rs7637619	0.85[EUR][1000 genomes]
rs7647576	0.86[EUR][1000 genomes]
rs9289839	0.91[EUR][1000 genomes]
rs9289847	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9289849	0.82[EUR][1000 genomes]
rs9680970	0.86[EUR][1000 genomes]
rs9683349	0.85[EUR][1000 genomes]
rs9808949	0.92[EUR][1000 genomes]
rs9811565	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9817125	1.00[CEU][hapmap];0.86[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9822315	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9836445	0.86[EUR][1000 genomes]
rs9837972	0.85[EUR][1000 genomes]
rs9846323	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9849929	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9850195	0.82[EUR][1000 genomes]
rs9856077	0.88[EUR][1000 genomes]
rs9863245	0.92[EUR][1000 genomes]
rs9883254	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829757	chr3:151044880-151226442	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1000355	chr3:151108859-151243835	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv995048	chr3:151114074-151560019	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
4	nsv877649	chr3:151147968-151236562	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv877650	chr3:151174010-151314449	Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv819466	chr3:151196634-151219966	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
7	nsv528372	chr3:151210190-151218277	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:151217200-151217800	Enhancers	Ovary	ovary
2	chr3:151217200-151218400	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr3:151217200-151218600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr3:151217400-151218400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr3:151217400-151219200	Weak transcription	Fetal Lung	lung
6	chr3:151217400-151219600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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