Variant report

Variant	rs4428006
Chromosome Location	chr2:67611053-67611054
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:67609713..67611781-chr2:67617304..67619056,2	K562	blood:
2	chr2:67608824..67611674-chr2:67618385..67620803,2	MCF-7	breast:

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10496153	0.87[EUR][1000 genomes]
rs1063571	0.85[EUR][1000 genomes]
rs12185591	0.85[EUR][1000 genomes]
rs12185702	0.85[EUR][1000 genomes]
rs12988210	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12991090	0.84[EUR][1000 genomes]
rs12996359	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13000557	0.84[EUR][1000 genomes]
rs13004747	0.84[EUR][1000 genomes]
rs13004765	0.84[EUR][1000 genomes]
rs13009070	0.88[EUR][1000 genomes]
rs13015319	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13015349	0.84[EUR][1000 genomes]
rs13016330	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13016336	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13017696	0.85[EUR][1000 genomes]
rs13018272	0.88[AMR][1000 genomes]
rs13018894	0.84[EUR][1000 genomes]
rs13026513	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13030037	0.85[EUR][1000 genomes]
rs13030211	0.85[EUR][1000 genomes]
rs13034744	0.84[EUR][1000 genomes]
rs13035051	0.83[EUR][1000 genomes]
rs13035754	0.84[EUR][1000 genomes]
rs13036061	0.87[EUR][1000 genomes]
rs1521051	0.81[EUR][1000 genomes]
rs17544516	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17544551	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17545245	0.85[EUR][1000 genomes]
rs17545301	0.85[EUR][1000 genomes]
rs17545329	0.85[EUR][1000 genomes]
rs17603914	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2171176	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34103917	0.85[EUR][1000 genomes]
rs34274370	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34281542	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34418651	0.82[EUR][1000 genomes]
rs34493710	0.85[EUR][1000 genomes]
rs34547630	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34636997	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34737312	0.88[EUR][1000 genomes]
rs34920978	0.84[EUR][1000 genomes]
rs34962808	0.84[EUR][1000 genomes]
rs34997300	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35002490	0.82[EUR][1000 genomes]
rs35141978	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35144434	0.85[EUR][1000 genomes]
rs35340993	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35382600	0.85[EUR][1000 genomes]
rs35503819	0.85[EUR][1000 genomes]
rs35570926	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35593975	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35607813	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35610403	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35686078	0.84[EUR][1000 genomes]
rs35777125	0.88[EUR][1000 genomes]
rs36098430	0.85[EUR][1000 genomes]
rs62154898	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62154948	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62154949	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62154950	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62154951	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62154952	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62154955	0.88[EUR][1000 genomes]
rs62154957	0.88[EUR][1000 genomes]
rs62154958	0.88[EUR][1000 genomes]
rs62156688	0.84[EUR][1000 genomes]
rs62156689	0.85[EUR][1000 genomes]
rs62156692	0.85[EUR][1000 genomes]
rs62156693	0.84[EUR][1000 genomes]
rs62156695	0.85[EUR][1000 genomes]
rs62156696	0.84[EUR][1000 genomes]
rs62156698	0.84[EUR][1000 genomes]
rs62156699	0.85[EUR][1000 genomes]
rs62156700	0.85[EUR][1000 genomes]
rs62156702	0.85[EUR][1000 genomes]
rs62156703	0.85[EUR][1000 genomes]
rs62156754	0.85[EUR][1000 genomes]
rs62156756	0.82[EUR][1000 genomes]
rs62156757	0.82[EUR][1000 genomes]
rs62156758	0.82[EUR][1000 genomes]
rs62158289	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62158290	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6710099	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6725762	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71411986	0.80[EUR][1000 genomes]
rs7585807	0.84[EUR][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	nsv1008584	chr2:67168244-67703601	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv535775	chr2:67168244-67703601	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv834249	chr2:67515471-67691605	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	esv3335541	chr2:67577544-67773907	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67600000-67611600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:67601800-67616200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr2:67602200-67615600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr2:67602200-67615800	Weak transcription	HUVEC	blood vessel
5	chr2:67602200-67617000	Weak transcription	Aorta	Aorta
6	chr2:67602600-67615800	Weak transcription	NHLF	lung
7	chr2:67606600-67624200	Weak transcription	Pancreas	Pancrea
8	chr2:67611000-67615800	Weak transcription	NH-A	brain

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