Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:16499530..16502497-chr7:16557938..16560776,2	K562	blood:
2	chr7:16459174..16462298-chr7:16499755..16502845,3	K562	blood:
3	chr7:16499817..16502074-chr7:16502589..16505491,4	K562	blood:

Variant related genes	Relation type
ENSG00000171243	Chromatin interaction
ENSG00000214960	Chromatin interaction

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10085439	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10085489	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10085777	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10499469	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs11766828	0.99[ASN][1000 genomes]
rs11770398	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs12532480	0.90[CHB][hapmap];0.91[JPT][hapmap]
rs12668183	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12699796	0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12699798	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs12699800	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs12699801	0.93[ASN][1000 genomes]
rs12699802	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs17619106	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs2141804	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs2293672	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs2301971	0.90[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4719466	0.90[CHB][hapmap];0.95[JPT][hapmap]
rs4721504	0.91[CHB][hapmap];0.91[JPT][hapmap]
rs56271810	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6461257	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6964287	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7798302	0.98[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8180829	0.83[AMR][1000 genomes];0.90[EUR][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	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv2759514	chr7:16236162-16527390	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2758105	chr7:16272822-16527390	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv1034151	chr7:16415497-16578081	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 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	chr7:16496200-16501000	Weak transcription	Fetal Kidney	kidney
2	chr7:16498600-16500800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:16498800-16500600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr7:16500400-16502000	Enhancers	Breast Myoepithelial Primary Cells	Breast

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