Variant report

Variant	rs17036992
Chromosome Location	chr4:159032644-159032645
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:159031275..159033687-chr4:159053603..159055452,2	MCF-7	breast:
2	chr4:159015350..159017695-chr4:159032159..159035060,3	MCF-7	breast:

Extended variants
information (count: 71 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs10021199	1.00[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10517685	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10517686	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11100152	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11933839	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11939690	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13130880	0.86[ASN][1000 genomes]
rs13137328	0.86[ASN][1000 genomes]
rs13137541	0.86[ASN][1000 genomes]
rs17036995	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17037201	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes]
rs17037232	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes]
rs17212066	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17212714	0.91[CEU][hapmap];1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17271385	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17279270	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes]
rs2594759	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2594760	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2725492	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs2725504	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2725505	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2725506	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2725507	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2725508	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs2881374	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4234916	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs4443327	0.86[ASN][1000 genomes]
rs4508943	1.00[CHB][hapmap]
rs4510503	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs4549446	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs4608853	0.86[ASN][1000 genomes]
rs6536289	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap]
rs6536290	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs6536294	0.86[ASN][1000 genomes]
rs6815974	0.86[ASN][1000 genomes]
rs6820988	1.00[CEU][hapmap];0.80[EUR][1000 genomes]
rs6834839	0.91[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes]
rs6837943	0.90[CEU][hapmap];1.00[CHB][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes]
rs72691603	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72691606	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72691610	0.81[EUR][1000 genomes]
rs72691615	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691620	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691622	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691626	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691627	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691629	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691631	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691632	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691633	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691634	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691636	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72691649	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72695726	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72695736	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72695741	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72695744	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs72695745	0.90[EUR][1000 genomes]
rs72695747	0.90[EUR][1000 genomes]
rs72695748	0.90[EUR][1000 genomes]
rs72695749	0.90[EUR][1000 genomes]
rs72695750	0.90[EUR][1000 genomes]
rs72695751	0.90[EUR][1000 genomes]
rs72695753	0.90[EUR][1000 genomes]
rs7664129	0.86[ASN][1000 genomes]
rs7678302	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs9997618	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[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	nsv993476	chr4:158550643-159202015	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1030124	chr4:158758675-159251140	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv1021067	chr4:158972282-159175475	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv880293	chr4:159012365-159049020	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs17036992	DKFZp434L142	cis	multi-tissue	Pritchard
rs17036992	FLJ11155	cis	multi-tissue	Pritchard
rs17036992	RP11-597D13.9	cis	Skin Sun Exposed Lower leg	GTEx
rs17036992	TMEM144	cis	Esophagus Muscularis	GTEx
rs17036992	RP11-597D13.9	cis	Esophagus Muscularis	GTEx

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:159030000-159034000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr4:159031400-159042000	Weak transcription	Fetal Heart	heart
3	chr4:159031600-159033000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:159031800-159036200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:159032000-159033800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:159032200-159032800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr4:159032400-159033600	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:159032600-159035600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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