Variant report

Variant	rs310260
Chromosome Location	chr6:70291892-70291893
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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

rs_ID	r²[population]
rs2572991	0.86[AFR][1000 genomes];0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2607730	0.93[ASN][1000 genomes]
rs2757757	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2757758	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs310259	0.85[ASN][1000 genomes]
rs34857559	0.83[ASN][1000 genomes]
rs4707218	0.84[ASN][1000 genomes]
rs6904921	0.91[CHB][hapmap];0.96[JPT][hapmap]
rs9351764	0.83[ASN][1000 genomes]
rs9364032	0.95[ASN][1000 genomes]
rs9364033	0.84[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70288800-70293600	Weak transcription	HSMMtube	muscle
2	chr6:70289000-70292800	Weak transcription	HSMM	muscle
3	chr6:70289000-70294400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:70289000-70294400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:70290400-70292000	Enhancers	Fetal Brain Female	brain
6	chr6:70291200-70293400	Weak transcription	Fetal Heart	heart
7	chr6:70291600-70294400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:70291800-70294800	Weak transcription	Fetal Brain Male	brain

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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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