Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:21497861..21500462-chr4:21501332..21503199,2	K562	blood:

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10014209	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10516387	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16871128	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16871243	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs17464007	0.80[CEU][hapmap]
rs17523974	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1903320	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28850130	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs358591	0.88[CEU][hapmap]
rs56989378	0.86[ASN][1000 genomes]
rs57335220	0.86[ASN][1000 genomes]
rs60294689	0.86[ASN][1000 genomes]
rs6846958	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs73105830	0.86[ASN][1000 genomes]
rs73105834	0.86[ASN][1000 genomes]
rs73105836	0.86[ASN][1000 genomes]
rs73105840	0.86[ASN][1000 genomes]
rs73105849	0.86[ASN][1000 genomes]
rs73105853	0.86[ASN][1000 genomes]
rs73105855	0.86[ASN][1000 genomes]
rs73105858	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013365	chr4:20834054-21609078	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
2	nsv829879	chr4:21418568-21611002	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv998481	chr4:21421945-21608805	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv829880	chr4:21492426-21693816	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv878750	chr4:21492445-21520250	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21497000-21514200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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