Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:104945753..104947544-chr8:104999072..105000833,2	K562	blood:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs12677553	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12678453	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12678653	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12681340	0.83[AFR][1000 genomes]
rs16870667	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16870704	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs16870797	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16870817	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16870822	0.94[ASN][1000 genomes]
rs16870826	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs16870841	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17854256	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17854257	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2023031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4531015	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72685005	0.83[AFR][1000 genomes]
rs72685006	0.83[AFR][1000 genomes]
rs72685007	0.83[AFR][1000 genomes]
rs72685013	0.83[AFR][1000 genomes]
rs72685015	0.83[AFR][1000 genomes]
rs73699003	0.97[ASN][1000 genomes]
rs73699004	0.97[ASN][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	esv2752692	chr8:104520824-105123824	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv1031195	chr8:104601231-105194208	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
3	nsv831415	chr8:104907757-105115320	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:104929400-104949600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr8:104930000-104949400	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr8:104938000-104949800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr8:104939000-104948600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr8:104939000-104951400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr8:104939000-104955200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:104939400-104959600	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:104945000-104948800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:104945800-104949400	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr8:104946200-104949600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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