Variant report

Variant	rs10850906
Chromosome Location	chr12:118258866-118258867
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs12318877	0.91[EUR][1000 genomes]
rs17439762	1.00[ASN][1000 genomes]
rs61939865	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7309589	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7358657	0.94[EUR][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118253800-118266400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:118254200-118264000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:118256200-118260600	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr12:118256600-118266400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr12:118257200-118266400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:118258200-118259000	Enhancers	Rectal Mucosa Donor 29	rectum

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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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