Variant report

Variant	rs7751008
Chromosome Location	chr6:145669784-145669785
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2328653	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs6916020	0.92[CEU][hapmap];0.89[CHB][hapmap];0.96[JPT][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6927602	0.83[EUR][1000 genomes]
rs7751694	0.92[ASN][1000 genomes]
rs9386112	0.84[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145668200-145670400	Enhancers	GM12878-XiMat	blood
2	chr6:145669000-145669800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr6:145669200-145669800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:145669400-145670000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr6:145669400-145671400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr6:145669400-145671600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr6:145669600-145670200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr6:145669600-145671000	Weak transcription	iPS-15b Cell Line	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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