Variant report

Variant	rs73488760
Chromosome Location	chr11:74918095-74918096
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs17133818	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17133831	0.88[ASN][1000 genomes]
rs17133844	0.88[ASN][1000 genomes]
rs17133848	0.88[ASN][1000 genomes]
rs1801906	0.87[ASN][1000 genomes]
rs2035208	0.88[ASN][1000 genomes]
rs3781726	0.91[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3781727	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs41298121	0.87[ASN][1000 genomes]
rs56253315	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs56738638	0.88[ASN][1000 genomes]
rs57279023	0.88[ASN][1000 genomes]
rs58769063	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61443691	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73488764	0.88[ASN][1000 genomes]
rs7924924	0.88[ASN][1000 genomes]
rs7951787	0.88[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74911400-74919800	Weak transcription	Spleen	Spleen
2	chr11:74915800-74919600	Weak transcription	Lung	lung
3	chr11:74916000-74918600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:74916000-74919600	Weak transcription	Pancreas	Pancrea
5	chr11:74916000-74920800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:74916400-74918600	Weak transcription	Fetal Muscle Leg	muscle
7	chr11:74916400-74919200	Weak transcription	K562	blood
8	chr11:74916800-74919600	Weak transcription	Liver	Liver
9	chr11:74917200-74919800	Weak transcription	Fetal Intestine Small	intestine
10	chr11:74917200-74920400	Weak transcription	Fetal Intestine Large	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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