Variant report

Variant	rs9403668
Chromosome Location	chr6:145528446-145528447
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12174179	1.00[ASN][1000 genomes]
rs28729387	0.81[ASN][1000 genomes]
rs9376902	1.00[ASN][1000 genomes]
rs9376904	0.81[ASN][1000 genomes]
rs9386105	0.88[ASN][1000 genomes]
rs9390291	1.00[ASN][1000 genomes]
rs9390292	0.81[ASN][1000 genomes]
rs9399537	1.00[ASN][1000 genomes]
rs9399538	0.83[ASN][1000 genomes]
rs9403670	0.97[ASN][1000 genomes]
rs9403674	1.00[ASN][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	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1022965	chr6:145374851-145635385	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv830834	chr6:145392073-145556294	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv886745	chr6:145494486-145554124	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145526800-145528600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr6:145527200-145528600	Enhancers	Osteobl	bone
3	chr6:145527800-145528800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:145527800-145529000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr6:145528200-145528800	Enhancers	NHDF-Ad	bronchial
6	chr6:145528200-145531600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr6:145528400-145530400	Weak transcription	Adipose Nuclei	Adipose
8	chr6:145528400-145530800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr6:145528400-145535800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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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