Variant report

Variant	rs74158274
Chromosome Location	chr10:117498718-117498719
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11197425	1.00[AMR][1000 genomes]
rs11814391	1.00[AMR][1000 genomes]
rs11815570	1.00[AMR][1000 genomes]
rs11819600	1.00[AMR][1000 genomes]
rs12242852	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12244147	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12251850	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12251879	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12253441	1.00[AMR][1000 genomes]
rs12255338	1.00[AMR][1000 genomes]
rs12258177	1.00[AMR][1000 genomes]
rs12262485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12262493	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12269265	1.00[AMR][1000 genomes]
rs56364264	1.00[AMR][1000 genomes]
rs56379384	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7070325	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7080508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7095980	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7099966	1.00[AMR][1000 genomes]
rs74158241	1.00[AMR][1000 genomes]
rs74158276	1.00[AMR][1000 genomes]
rs74158277	1.00[AMR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117489400-117520800	Weak transcription	HSMM	muscle
2	chr10:117490800-117509600	Weak transcription	Aorta	Aorta
3	chr10:117498600-117498800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr10:117498600-117499000	Enhancers	Fetal Brain Female	brain

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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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