Variant report

Variant	rs45562238
Chromosome Location	chr6:133013544-133013545
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs11154689	1.00[ASN][1000 genomes]
rs17061798	1.00[ASN][1000 genomes]
rs17606700	1.00[ASN][1000 genomes]
rs2745425	1.00[ASN][1000 genomes]
rs45530734	1.00[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	nsv532069	chr6:132776411-133462292	Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1015742	chr6:132933666-133285852	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133002200-133014600	Strong transcription	Liver	Liver
2	chr6:133004800-133016400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:133008800-133016200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr6:133010400-133015200	Strong transcription	Primary neutrophils fromperipheralblood	blood
5	chr6:133010800-133013800	Strong transcription	Duodenum Mucosa	Duodenum
6	chr6:133011000-133015200	Strong transcription	Monocytes-CD14+_RO01746	blood
7	chr6:133011200-133015000	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr6:133011600-133014200	Weak transcription	Pancreas	Pancrea
9	chr6:133011800-133017200	Weak transcription	Spleen	Spleen
10	chr6:133012600-133015000	Weak transcription	Stomach Mucosa	stomach
11	chr6:133013000-133015000	Weak transcription	Primary hematopoietic stem cells	blood

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

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