Variant report

Variant	rs6936918
Chromosome Location	chr6:11530613-11530614
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10046197	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1150563	1.00[EUR][1000 genomes]
rs1150569	1.00[EUR][1000 genomes]
rs1195651	1.00[EUR][1000 genomes]
rs11962713	1.00[EUR][1000 genomes]
rs12332876	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2807965	1.00[EUR][1000 genomes]
rs295057	1.00[EUR][1000 genomes]
rs477973	1.00[EUR][1000 genomes]
rs544766	1.00[EUR][1000 genomes]
rs552548	1.00[EUR][1000 genomes]
rs585322	1.00[EUR][1000 genomes]
rs58716971	1.00[EUR][1000 genomes]
rs59791855	1.00[EUR][1000 genomes]
rs609389	1.00[EUR][1000 genomes]
rs613353	1.00[EUR][1000 genomes]
rs61378967	1.00[EUR][1000 genomes]
rs61679516	1.00[EUR][1000 genomes]
rs617146	1.00[EUR][1000 genomes]
rs656674	1.00[EUR][1000 genomes]
rs6940009	1.00[EUR][1000 genomes]
rs73351939	1.00[EUR][1000 genomes]
rs73351942	1.00[EUR][1000 genomes]
rs73351967	1.00[EUR][1000 genomes]
rs73351970	1.00[EUR][1000 genomes]
rs73351978	1.00[EUR][1000 genomes]
rs73351980	1.00[EUR][1000 genomes]
rs73355853	1.00[EUR][1000 genomes]
rs73368833	1.00[EUR][1000 genomes]
rs7744252	1.00[EUR][1000 genomes]
rs7744403	1.00[EUR][1000 genomes]
rs7761428	1.00[EUR][1000 genomes]
rs821537	1.00[EUR][1000 genomes]
rs821541	1.00[EUR][1000 genomes]

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	nsv1021078	chr6:10819083-11558560	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers 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 miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv538135	chr6:10819083-11558560	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv432848	chr6:11371614-11560114	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv600989	chr6:11509323-11581990	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11522000-11536400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:11526800-11531600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr6:11527000-11532600	Weak transcription	Adipose Nuclei	Adipose
4	chr6:11527000-11537000	Weak transcription	Placenta	Placenta
5	chr6:11527400-11531000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:11527400-11531600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:11527400-11537200	Weak transcription	Gastric	stomach
8	chr6:11528000-11530800	Weak transcription	Primary neutrophils fromperipheralblood	blood
9	chr6:11528000-11531200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr6:11528000-11536800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:11530600-11531200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:11530600-11531200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr6:11530600-11531400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:11530600-11531800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:11530600-11532000	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr6:11530600-11532000	Enhancers	Monocytes-CD14+_RO01746	blood

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