Variant report

Variant	rs1102838
Chromosome Location	chr1:85196303-85196304
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1093622	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12095186	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2911575	0.86[AMR][1000 genomes]
rs2911583	0.89[AMR][1000 genomes]
rs3768238	0.89[AMR][1000 genomes]
rs4390189	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4551615	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs56681543	0.89[AMR][1000 genomes]
rs6576722	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6670434	0.86[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85190600-85199800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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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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