Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:79166906..79168962-chr14:79171099..79172948,2	K562	blood:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10131453	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10146003	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs11624715	1.00[JPT][hapmap]
rs12882483	1.00[CEU][hapmap]
rs12886193	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12886874	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1465481	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2113574	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2194531	1.00[CEU][hapmap]
rs2241440	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2887859	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4903790	0.92[ASN][1000 genomes]
rs6574465	1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6574466	1.00[JPT][hapmap]
rs6574467	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7141190	1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs7144972	1.00[JPT][hapmap]
rs7146256	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7148486	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7148791	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7150071	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs7153536	1.00[JPT][hapmap]
rs8008196	1.00[JPT][hapmap]
rs8008442	0.98[ASN][1000 genomes]
rs8013926	1.00[JPT][hapmap]
rs8015985	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs8181983	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:79165000-79176800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr14:79165000-79181000	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr14:79170600-79173200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr14:79170800-79176600	Weak transcription	Brain Hippocampus Middle	brain
5	chr14:79171400-79173000	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr14:79171800-79175600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr14:79171800-79175600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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