Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:37535319..37537304-chr14:37555545..37557530,2	K562	blood:

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1012198	0.82[CEU][hapmap]
rs10132328	0.93[EUR][1000 genomes]
rs10134406	0.82[CEU][hapmap]
rs10141752	1.00[CEU][hapmap]
rs10148774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10220281	0.93[EUR][1000 genomes]
rs10220604	0.82[CEU][hapmap]
rs1057564	0.82[CEU][hapmap]
rs12717260	0.98[EUR][1000 genomes]
rs12889634	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs17106209	0.82[CEU][hapmap]
rs17106216	0.82[CEU][hapmap]
rs17178639	0.82[CEU][hapmap]
rs17178764	0.82[CEU][hapmap]
rs17767749	0.82[CEU][hapmap]
rs17767929	0.82[CEU][hapmap]
rs1884775	0.82[CEU][hapmap]
rs1884777	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1950377	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1950814	0.82[CEU][hapmap]
rs1955758	0.82[CEU][hapmap]
rs1955760	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1956423	0.82[CEU][hapmap]
rs2057171	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs2415379	0.82[CEU][hapmap]
rs2415386	0.82[CEU][hapmap]
rs4363773	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6571781	0.82[CEU][hapmap]
rs6571782	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6571785	0.82[CEU][hapmap]
rs7151524	0.82[CEU][hapmap]
rs725243	0.82[CEU][hapmap]
rs8009630	0.82[CEU][hapmap]
rs8012664	0.82[CEU][hapmap]
rs8014186	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs8019489	0.82[CEU][hapmap]
rs8020153	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs976171	0.82[CEU][hapmap]

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	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1050174	chr14:37556357-37664143	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1043410	chr14:37556357-37671059	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37553400-37562600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:37553600-37557800	Weak transcription	Pancreas	Pancrea
3	chr14:37557200-37558000	Enhancers	K562	blood

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