Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:69666329..69668824-chr8:69675857..69677565,2	K562	blood:

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10110245	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10957446	0.84[CHB][hapmap];0.92[JPT][hapmap]
rs11987041	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4299986	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4484685	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4621793	0.93[YRI][hapmap]
rs6472419	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs6990164	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs719689	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs719690	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7821966	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7822136	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7822340	1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7826665	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7826725	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7826997	1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831349	chr8:69555461-69733515	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv465703	chr8:69641287-69814578	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv611462	chr8:69641287-69814578	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv890986	chr8:69647914-69704366	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:69640200-69676800	Weak transcription	Aorta	Aorta
2	chr8:69672600-69676200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:69672600-69676200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr8:69672600-69676600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:69673000-69676800	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr8:69673200-69676600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr8:69673200-69676600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr8:69673200-69679800	Weak transcription	HUVEC	blood vessel
9	chr8:69673400-69676600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:69673600-69676600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr8:69673600-69678200	Weak transcription	HMEC	breast
12	chr8:69673800-69676200	Weak transcription	Hela-S3	cervix
13	chr8:69673800-69679800	Weak transcription	Osteobl	bone
14	chr8:69673800-69682000	Weak transcription	HSMMtube	muscle
15	chr8:69674400-69676600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr8:69674400-69676600	Weak transcription	HSMM	muscle
17	chr8:69674400-69679800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr8:69674400-69679800	Weak transcription	NHLF	lung
19	chr8:69674800-69682000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr8:69675200-69686200	Weak transcription	Fetal Lung	lung

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