Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:119035847..119037394-chr12:119041054..119043149,2	K562	blood:

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

rs_ID	r²[population]
rs10851010	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11069000	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11069047	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12298592	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12309659	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13377697	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1566415	1.00[ASN][1000 genomes]
rs17441179	1.00[ASN][1000 genomes]
rs1814734	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1879405	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4767701	0.82[EUR][1000 genomes]
rs55753185	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56345501	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57022566	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57408027	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs58438786	1.00[ASN][1000 genomes]
rs7137265	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7296420	0.82[EUR][1000 genomes]
rs7303736	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73411684	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73415208	0.91[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73415220	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7973816	0.89[AFR][1000 genomes]
rs937528	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv930978	chr12:118866332-119450600	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv1043906	chr12:118991884-119087146	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	esv3441208	chr12:119041969-119046367	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119040800-119042600	Enhancers	HepG2	liver
2	chr12:119041200-119042800	Enhancers	Pancreas	Pancrea
3	chr12:119041800-119046400	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr12:119042200-119047600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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