Variant report

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

rs_ID	r²[population]
rs10484809	0.80[ASN][1000 genomes]
rs12662099	0.86[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs12662559	0.86[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs12662669	0.80[ASN][1000 genomes]
rs12664697	0.86[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs12665178	0.82[CHB][hapmap];1.00[JPT][hapmap]
rs2361500	0.81[CHD][hapmap];1.00[JPT][hapmap]
rs2878176	0.94[ASN][1000 genomes]
rs3806158	0.81[CHD][hapmap];1.00[JPT][hapmap]
rs3828928	0.81[CHD][hapmap];1.00[JPT][hapmap]
rs56798260	0.80[ASN][1000 genomes]
rs6918158	0.86[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap]
rs6927464	0.90[CHD][hapmap];1.00[JPT][hapmap]
rs6935544	0.81[CHD][hapmap];1.00[JPT][hapmap]
rs6937364	1.00[JPT][hapmap]
rs6940347	0.81[CHD][hapmap];1.00[JPT][hapmap]
rs7749049	0.80[ASN][1000 genomes]
rs7761025	0.80[ASN][1000 genomes]
rs7771649	1.00[JPT][hapmap]
rs9487324	0.86[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9688851	0.80[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	nsv948824	chr6:110443685-110889332	Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv949643	chr6:110537685-110889332	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	esv1847660	chr6:110606987-110985314	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:110605000-110617400	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr6:110605400-110617200	Weak transcription	Colon Smooth Muscle	Colon
3	chr6:110606800-110612400	Weak transcription	Ovary	ovary
4	chr6:110608000-110616600	Weak transcription	Fetal Stomach	stomach
5	chr6:110609200-110616400	Weak transcription	Aorta	Aorta
6	chr6:110609400-110617000	Weak transcription	Fetal Kidney	kidney
7	chr6:110609400-110632000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:110610000-110632200	Weak transcription	Pancreas	Pancrea
9	chr6:110610200-110617000	Weak transcription	Stomach Smooth Muscle	stomach

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