Variant report

Variant	rs926163
Chromosome Location	chr4:103364762-103364763
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000109332	Chromatin interaction
ENSG00000109320	Chromatin interaction
ENSG00000246560	Chromatin interaction
ENSG00000260651	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11097783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12510679	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12513242	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13115343	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13119968	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13132193	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17825737	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap]
rs17825838	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4699028	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6817730	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6846971	1.00[CHB][hapmap];1.00[JPT][hapmap]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103361400-103368200	Weak transcription	Primary hematopoietic stem cells	blood
2	chr4:103361400-103369400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:103363800-103365400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:103364200-103366400	Enhancers	Liver	Liver
5	chr4:103364200-103366400	Enhancers	HepG2	liver
6	chr4:103364400-103364800	Enhancers	K562	blood

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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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