Variant report

Variant	rs73380905
Chromosome Location	chr10:91414544-91414545
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs59230990	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7090819	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73378990	0.85[AFR][1000 genomes]
rs73379000	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73380903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73380935	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73380937	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73386467	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74147643	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91406600-91415800	Weak transcription	Colonic Mucosa	Colon
2	chr10:91407200-91418400	Weak transcription	Psoas Muscle	Psoas
3	chr10:91409000-91418800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr10:91412400-91415800	Enhancers	HepG2	liver
5	chr10:91413400-91414600	Weak transcription	Fetal Intestine Large	intestine
6	chr10:91413600-91416800	Weak transcription	Osteobl	bone
7	chr10:91413800-91418400	Weak transcription	NH-A	brain
8	chr10:91414000-91417400	ZNF genes & repeats	Fetal Intestine Small	intestine
9	chr10:91414200-91415000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:91414400-91414600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:91414400-91416200	ZNF genes & repeats	Primary B cells from peripheral blood	blood

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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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