Variant report

Variant	rs12127573
Chromosome Location	chr1:71219037-71219038
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10493478	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12048393	0.86[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12141116	0.88[CEU][hapmap]
rs2152126	0.86[CEU][hapmap]
rs2782770	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61778712	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6685675	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs950031	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71217800-71219200	Enhancers	Placenta	Placenta
2	chr1:71218600-71219200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:71218600-71219400	Enhancers	Placenta Amnion	Placenta Amnion
4	chr1:71218800-71219400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr1:71218800-71221800	Enhancers	K562	blood

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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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