Variant report

Variant	rs12662422
Chromosome Location	chr6:38278913-38278914
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11758664	1.00[ASN][1000 genomes]
rs12660215	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12661843	1.00[ASN][1000 genomes]
rs12664020	0.84[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13193103	1.00[ASN][1000 genomes]
rs13197522	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13198868	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13206261	1.00[ASN][1000 genomes]
rs13209118	1.00[ASN][1000 genomes]
rs16890541	1.00[ASN][1000 genomes]
rs28360643	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36094313	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60814959	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62397020	1.00[ASN][1000 genomes]
rs6907434	1.00[ASN][1000 genomes]
rs71571312	1.00[ASN][1000 genomes]
rs7762070	1.00[ASN][1000 genomes]
rs7768902	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021991	chr6:37893949-38738720	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	nsv534620	chr6:38049585-38602064	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv885818	chr6:38147745-38436317	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv885820	chr6:38166511-38468887	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38274400-38288600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr6:38275400-38301200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr6:38276000-38286200	Weak transcription	Primary T cells from cord blood	blood
4	chr6:38276000-38287600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr6:38276000-38287800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr6:38276200-38286800	Weak transcription	HSMMtube	muscle
7	chr6:38277800-38279000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:38278000-38310600	Weak transcription	Gastric	stomach
9	chr6:38278200-38283000	Weak transcription	GM12878-XiMat	blood
10	chr6:38278200-38288000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr6:38278200-38295000	Weak transcription	Lung	lung
12	chr6:38278400-38305400	Weak transcription	Pancreas	Pancrea

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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