Variant report

Variant	rs10268028
Chromosome Location	chr7:137910548-137910549
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11764095	0.94[ASN][1000 genomes]
rs11771184	0.89[ASN][1000 genomes]
rs13221468	0.92[ASN][1000 genomes]
rs13221578	0.92[ASN][1000 genomes]
rs13221616	0.92[ASN][1000 genomes]
rs13228035	0.93[ASN][1000 genomes]
rs13228776	0.92[ASN][1000 genomes]
rs13230213	0.90[ASN][1000 genomes]
rs13234577	1.00[ASN][1000 genomes]
rs1387585	0.92[ASN][1000 genomes]
rs2352477	0.85[ASN][1000 genomes]
rs2352478	0.84[ASN][1000 genomes]
rs34230550	0.92[ASN][1000 genomes]
rs34446043	0.91[ASN][1000 genomes]
rs34458644	0.93[ASN][1000 genomes]
rs34610374	0.90[ASN][1000 genomes]
rs4031456	0.93[ASN][1000 genomes]
rs4142644	0.92[ASN][1000 genomes]
rs4142645	0.92[ASN][1000 genomes]
rs57177181	0.92[ASN][1000 genomes]
rs57628314	0.92[ASN][1000 genomes]
rs59635163	0.92[ASN][1000 genomes]
rs6467745	0.83[EUR][1000 genomes]
rs6467746	0.88[EUR][1000 genomes]
rs6944836	0.98[ASN][1000 genomes]
rs6955437	0.92[ASN][1000 genomes]
rs6963150	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs6976623	0.90[ASN][1000 genomes]
rs71309397	0.92[ASN][1000 genomes]
rs73731511	0.92[ASN][1000 genomes]
rs7780731	0.92[ASN][1000 genomes]
rs7792003	0.94[ASN][1000 genomes]
rs7794151	0.92[ASN][1000 genomes]
rs7797681	0.92[ASN][1000 genomes]
rs7797842	0.92[ASN][1000 genomes]
rs7806666	0.92[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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831152	chr7:137884311-138033117	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137905800-137914800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:137905800-137928600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:137906800-137910600	Weak transcription	Pancreas	Pancrea
4	chr7:137907000-137910600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr7:137908600-137913600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:137909400-137911800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:137909400-137912200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:137910200-137910800	Weak transcription	Fetal Kidney	kidney
9	chr7:137910200-137911000	Enhancers	Liver	Liver
10	chr7:137910200-137911000	Enhancers	HepG2	liver

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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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