Variant report

Variant	rs41378151
Chromosome Location	chr1:176352039-176352040
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10798449	0.83[EUR][1000 genomes]
rs11801582	0.84[EUR][1000 genomes]
rs12125604	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs12126441	1.00[CEU][hapmap];0.95[GIH][hapmap];0.89[MEX][hapmap];0.92[TSI][hapmap];0.85[EUR][1000 genomes]
rs12137387	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12140384	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12143236	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12407844	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12408191	1.00[YRI][hapmap]
rs16849735	0.89[CEU][hapmap]
rs58715931	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs60617532	0.87[EUR][1000 genomes]
rs61821081	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs61821096	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:176348800-176353200	Enhancers	Fetal Intestine Large	intestine
2	chr1:176350600-176353600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr1:176351000-176353200	Enhancers	Fetal Intestine Small	intestine

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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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