Variant report

Variant	rs236852
Chromosome Location	chr6:79349892-79349893
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1012026	0.89[ASN][1000 genomes]
rs1012027	0.87[ASN][1000 genomes]
rs10455349	0.89[ASN][1000 genomes]
rs10806133	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs10943547	0.86[ASN][1000 genomes]
rs10943548	0.87[ASN][1000 genomes]
rs10943549	0.89[ASN][1000 genomes]
rs12197137	0.89[ASN][1000 genomes]
rs12201840	0.91[ASN][1000 genomes]
rs12209692	0.87[ASN][1000 genomes]
rs12210711	0.89[ASN][1000 genomes]
rs12213548	0.89[ASN][1000 genomes]
rs12530353	0.89[ASN][1000 genomes]
rs12530368	0.83[ASN][1000 genomes]
rs1395446	0.87[ASN][1000 genomes]
rs1395447	0.86[ASN][1000 genomes]
rs1407102	0.89[ASN][1000 genomes]
rs1567095	0.89[ASN][1000 genomes]
rs1567096	0.95[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs1567097	0.88[ASN][1000 genomes]
rs1570075	0.84[ASN][1000 genomes]
rs16890224	0.87[ASN][1000 genomes]
rs16890230	0.87[ASN][1000 genomes]
rs1995650	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs2063045	0.89[ASN][1000 genomes]
rs2202588	0.94[ASN][1000 genomes]
rs2321764	0.89[ASN][1000 genomes]
rs236853	0.89[ASN][1000 genomes]
rs236855	0.89[ASN][1000 genomes]
rs236859	0.89[ASN][1000 genomes]
rs236882	0.95[CHB][hapmap];0.90[JPT][hapmap];0.85[ASN][1000 genomes]
rs236884	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs236886	0.87[ASN][1000 genomes]
rs5018093	0.90[ASN][1000 genomes]
rs699182	0.87[ASN][1000 genomes]
rs717364	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs7755578	0.91[ASN][1000 genomes]
rs7763429	0.97[ASN][1000 genomes]
rs9361413	0.97[ASN][1000 genomes]
rs9361414	0.97[ASN][1000 genomes]
rs984157	0.86[ASN][1000 genomes]

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	nsv886235	chr6:78861808-79369972	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv604011	chr6:79042990-79455282	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79349000-79350200	Enhancers	Duodenum Mucosa	Duodenum
2	chr6:79349200-79350200	Enhancers	Fetal Intestine Small	intestine

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