Variant report

Variant	rs849302
Chromosome Location	chr7:106672772-106672773
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs2536489	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2536490	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs2536491	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2536497	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2536499	0.83[AMR][1000 genomes]
rs73413343	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106670200-106676800	Weak transcription	Fetal Brain Male	brain
2	chr7:106670800-106674000	Weak transcription	Fetal Heart	heart
3	chr7:106672200-106673600	Flanking Active TSS	K562	blood
4	chr7:106672400-106672800	ZNF genes & repeats	Pancreas	Pancrea
5	chr7:106672600-106673400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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