Variant report

Variant	rs7183668
Chromosome Location	chr15:79256158-79256159
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11072819	0.86[CEU][hapmap];0.87[EUR][1000 genomes]
rs11635178	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2289700	0.80[CHB][hapmap]
rs4408506	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.85[MKK][hapmap];0.97[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4779153	0.86[EUR][1000 genomes]
rs7175091	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7175785	0.87[EUR][1000 genomes]
rs7177831	0.97[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs876941	0.87[CEU][hapmap];0.84[TSI][hapmap];0.87[EUR][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	esv33573	chr15:79053484-79293881	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers 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	nsv904433	chr15:79243571-79310288	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7183668	CTSH	Cis_1M	lymphoblastoid	RTeQTL
rs7183668	MORF4L1	cis	cerebellum	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:79244000-79263400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr15:79244000-79288000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr15:79250800-79263400	Weak transcription	Brain Hippocampus Middle	brain
4	chr15:79253000-79260400	Weak transcription	Pancreas	Pancrea
5	chr15:79253000-79265400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:79253800-79263400	Weak transcription	Brain Angular Gyrus	brain
7	chr15:79254200-79263400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr15:79255800-79256200	Enhancers	Stomach Mucosa	stomach
9	chr15:79256000-79256200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr15:79256000-79256400	Enhancers	K562	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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