Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:78405474..78407016-chr7:78415742..78418693,2	K562	blood:

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

rs_ID	r²[population]
rs11981818	0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs1207884	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs1207885	0.80[ASN][1000 genomes]
rs1207887	0.95[JPT][hapmap]
rs1209400	0.85[JPT][hapmap]
rs1209720	0.90[JPT][hapmap]
rs12705800	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2214557	0.95[JPT][hapmap]
rs246460	0.84[CEU][hapmap];0.82[CHB][hapmap];0.85[JPT][hapmap]
rs246462	0.84[CEU][hapmap];0.82[CHB][hapmap];0.85[JPT][hapmap]
rs37858	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs37859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs37861	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs37867	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs37876	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs37880	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs37883	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs37885	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs37886	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs41495	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs489403	0.85[JPT][hapmap]
rs763518	0.95[JPT][hapmap]

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	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv949647	chr7:78406281-78495913	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78416800-78418400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:78416800-78418400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:78416800-78418400	Enhancers	HMEC	breast
4	chr7:78417000-78418400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:78417000-78418400	Enhancers	NHEK	skin
6	chr7:78417200-78418200	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr7:78417600-78418200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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