Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:57072693..57075566-chr6:57131464..57133518,2	MCF-7	breast:
2	chr6:57132762..57133471-chr6:57189050..57190018,2	K562	blood:
3	chr6:57054788..57055522-chr6:57132728..57133505,2	K562	blood:
4	chr6:57128467..57134592-chr6:57180122..57183939,9	MCF-7	breast:

Variant related genes	Relation type
ENSG00000146143	Chromatin interaction

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10080526	0.95[ASN][1000 genomes]
rs10949013	0.93[CHB][hapmap];0.93[CHD][hapmap];0.85[ASN][1000 genomes]
rs10949014	0.93[CHB][hapmap];0.85[ASN][1000 genomes]
rs13210430	0.83[ASN][1000 genomes]
rs16888410	0.93[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[MEX][hapmap];0.90[ASN][1000 genomes]
rs16888420	0.95[ASN][1000 genomes]
rs16888435	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16888439	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs34331825	0.87[AFR][1000 genomes]
rs62415953	0.90[ASN][1000 genomes]
rs62415955	0.98[ASN][1000 genomes]
rs62415956	0.86[ASN][1000 genomes]
rs62418081	0.94[ASN][1000 genomes]
rs62418083	0.86[ASN][1000 genomes]
rs6900622	0.91[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs6905517	0.83[ASN][1000 genomes]
rs6905598	0.85[ASN][1000 genomes]
rs6906645	0.93[CHB][hapmap];0.91[CHD][hapmap];0.85[ASN][1000 genomes]
rs6918565	0.90[ASN][1000 genomes]
rs9475804	1.00[ASN][1000 genomes]
rs9475805	0.93[CHB][hapmap];0.90[CHD][hapmap];0.85[ASN][1000 genomes]
rs9475808	1.00[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	nsv491933	chr6:56177722-57171010	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats 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	51 gene(s)	inside rSNPs	diseases
2	nsv934026	chr6:56382056-57184218	Flanking Bivalent TSS/Enh Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv533050	chr6:56504480-57297586	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv1034095	chr6:57102042-57162808	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57131200-57133400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr6:57131200-57133400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:57132000-57133400	Enhancers	NHEK	skin
4	chr6:57132800-57133400	Enhancers	Muscle Satellite Cultured Cells	--

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