Variant report

Variant	rs10400018
Chromosome Location	chr10:61706814-61706815
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10509120	1.00[CEU][hapmap]
rs10994165	1.00[CEU][hapmap]
rs10994167	1.00[CEU][hapmap]
rs10994169	1.00[CEU][hapmap]
rs1171844	1.00[EUR][1000 genomes]
rs12250558	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs12259133	1.00[CEU][hapmap]
rs12413122	1.00[CEU][hapmap]
rs3099372	1.00[EUR][1000 genomes]
rs6479671	1.00[EUR][1000 genomes]
rs6479674	0.91[ASW][hapmap];1.00[CEU][hapmap];0.96[MKK][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7068392	0.84[MKK][hapmap]
rs7083694	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7085413	1.00[EUR][1000 genomes]
rs7090532	1.00[GIH][hapmap]
rs7907227	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7923833	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:61706400-61707000	Enhancers	HUES48 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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