Variant report

Variant	rs26194
Chromosome Location	chr5:35363958-35363959
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs183624	1.00[ASN][1000 genomes]
rs26192	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs26196	0.87[ASN][1000 genomes]
rs32748	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs420207	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs73084919	0.81[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35363600-35364200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr5:35363600-35367800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr5:35363800-35365000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr5:35363800-35367800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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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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