Variant report

Variant	rs192620453
Chromosome Location	chr10:95818989-95818990
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv825525	chr10:95818696-95819230	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:95803400-95819800	Weak transcription	Fetal Intestine Large	intestine
2	chr10:95806400-95822600	Weak transcription	Fetal Intestine Small	intestine
3	chr10:95813800-95821600	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr10:95814000-95828600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr10:95814200-95822800	Weak transcription	Aorta	Aorta
6	chr10:95814400-95824200	Weak transcription	Fetal Muscle Leg	muscle
7	chr10:95814400-95836400	Weak transcription	Psoas Muscle	Psoas
8	chr10:95815800-95824800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr10:95817200-95819600	Enhancers	A549	lung
10	chr10:95818200-95819600	Enhancers	Stomach Mucosa	stomach
11	chr10:95818800-95819200	Enhancers	Sigmoid Colon	Sigmoid Colon

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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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