Variant report

Variant	rs2237408
Chromosome Location	chr7:39414126-39414127
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10227915	0.97[ASN][1000 genomes]
rs13438025	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4623320	0.87[ASN][1000 genomes]
rs61105243	0.97[ASN][1000 genomes]
rs61543464	0.87[ASN][1000 genomes]
rs7801145	0.81[AMR][1000 genomes]
rs7807957	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39413800-39414400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:39413800-39414800	Enhancers	HepG2	liver

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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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