Variant report

Variant	rs9493265
Chromosome Location	chr6:132593501-132593502
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs13437273	0.83[AFR][1000 genomes]
rs7759103	1.00[AMR][1000 genomes]
rs9483413	1.00[AMR][1000 genomes]
rs9483419	1.00[AMR][1000 genomes]
rs9493249	0.83[AFR][1000 genomes]
rs9493255	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv970165	chr6:132593252-132594252	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132589600-132595800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:132590000-132595400	Weak transcription	Aorta	Aorta
3	chr6:132592400-132596000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr6:132592600-132595400	Weak transcription	Fetal Intestine Large	intestine
5	chr6:132592600-132595400	Weak transcription	Fetal Intestine Small	intestine
6	chr6:132592600-132595600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:132592600-132595800	Weak transcription	Fetal Muscle Leg	muscle
8	chr6:132592600-132596400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:132592800-132595400	Weak transcription	Stomach Mucosa	stomach
10	chr6:132593400-132594200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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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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