Variant report

Variant	rs6451634
Chromosome Location	chr5:42684937-42684938
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	chr5:42683652..42685586-chr9:133557490..133559325,2	MCF-7	breast:

Extended variants
information (count: 83 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10041108	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10041932	0.93[CEU][hapmap];0.94[EUR][1000 genomes]
rs10044117	0.95[EUR][1000 genomes]
rs10067153	1.00[CHB][hapmap]
rs10069861	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10440649	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10941582	1.00[ASN][1000 genomes]
rs10941588	1.00[ASN][1000 genomes]
rs1109882	1.00[ASN][1000 genomes]
rs11948120	1.00[ASN][1000 genomes]
rs11948463	0.93[CEU][hapmap];1.00[GIH][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];0.94[EUR][1000 genomes]
rs11957404	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12514437	1.00[ASN][1000 genomes]
rs13163126	1.00[ASN][1000 genomes]
rs13168440	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap]
rs13171019	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13175765	1.00[ASN][1000 genomes]
rs13182117	1.00[CHB][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13184352	1.00[CHB][hapmap]
rs13354167	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs28919899	0.81[EUR][1000 genomes]
rs28943882	1.00[CHB][hapmap]
rs34159518	1.00[ASN][1000 genomes]
rs34343411	0.92[EUR][1000 genomes]
rs35164552	1.00[ASN][1000 genomes]
rs35893798	1.00[ASN][1000 genomes]
rs4129472	1.00[CHB][hapmap]
rs4242122	1.00[ASN][1000 genomes]
rs4242123	1.00[ASN][1000 genomes]
rs4242124	1.00[ASN][1000 genomes]
rs4292454	1.00[CHB][hapmap]
rs4355531	0.91[EUR][1000 genomes]
rs4413537	0.93[CEU][hapmap];1.00[GIH][hapmap];0.81[MKK][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes]
rs4419597	0.93[CEU][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs4451056	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs4523007	0.91[EUR][1000 genomes]
rs4594864	0.87[CEU][hapmap];1.00[GIH][hapmap];0.91[TSI][hapmap];0.91[EUR][1000 genomes]
rs4866792	1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes]
rs4866793	1.00[ASN][1000 genomes]
rs4866943	1.00[EUR][1000 genomes]
rs4866944	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs4866955	1.00[ASN][1000 genomes]
rs4866956	1.00[ASN][1000 genomes]
rs4866957	1.00[ASN][1000 genomes]
rs4994772	1.00[CEU][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs5025611	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6413428	1.00[CHB][hapmap]
rs6414898	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6451632	1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6451633	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6451635	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs6451641	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6451643	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6863381	1.00[CHB][hapmap]
rs6871947	1.00[ASN][1000 genomes]
rs6873340	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6873794	1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6878461	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6878512	1.00[CEU][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs6894403	0.93[CEU][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7442690	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7444761	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7447731	1.00[CEU][hapmap];0.95[YRI][hapmap];0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7702524	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs7709370	1.00[ASN][1000 genomes]
rs7709790	1.00[CHB][hapmap]
rs7721081	1.00[CEU][hapmap];1.00[GIH][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes]
rs7722558	0.93[CEU][hapmap];1.00[GIH][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes]
rs9292854	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs9292855	0.95[EUR][1000 genomes]
rs9292856	1.00[CEU][hapmap];1.00[GIH][hapmap];0.80[MKK][hapmap];0.95[TSI][hapmap];0.95[EUR][1000 genomes]
rs9717120	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933208	chr5:41879946-42876624	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	112 gene(s)	inside rSNPs	diseases
2	nsv492147	chr5:41902086-42896162	Enhancers Flanking Active TSS Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	113 gene(s)	inside rSNPs	diseases
3	nsv1020464	chr5:42488628-42699394	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1018751	chr5:42491883-42697923	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1031160	chr5:42610090-42843255	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv1019696	chr5:42610090-42844191	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv597886	chr5:42610409-42854408	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1029933	chr5:42611976-42833385	Enhancers Transcr. at gene 5' and 3' Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv537735	chr5:42611976-42833385	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv1019648	chr5:42616487-42696943	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv537736	chr5:42616487-42696943	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6451634	SEPP1	cis	cerebellum	SCAN
rs6451634	XAGE3	trans	parietal	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42677000-42691600	Weak transcription	Aorta	Aorta
2	chr5:42679800-42691600	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr5:42680800-42688000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:42683000-42688600	Weak transcription	Adipose Nuclei	Adipose
5	chr5:42683000-42688800	Weak transcription	Fetal Lung	lung
6	chr5:42683000-42689000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr5:42683200-42691200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr5:42684200-42685000	Strong transcription	Liver	Liver
9	chr5:42684600-42688400	Weak transcription	Left Ventricle	heart
10	chr5:42684800-42685000	ZNF genes & repeats	Right Ventricle	heart

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