Variant report

Variant	rs10155472
Chromosome Location	chr4:190852887-190852888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs13136745	0.86[EUR][1000 genomes]
rs13136956	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13140896	0.89[EUR][1000 genomes]
rs6817914	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72642097	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10155472	AF146191.4	cis	Thyroid	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:190845000-190858200	Weak transcription	Gastric	stomach
2	chr4:190847600-190860800	Weak transcription	Pancreas	Pancrea
3	chr4:190848000-190856600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:190852200-190861200	Weak transcription	Fetal Intestine Large	intestine
5	chr4:190852400-190860800	Weak transcription	Skeletal Muscle Female	skeletal muscle

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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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