Variant report

Variant	rs397738128
Chromosome Location	chr1:84127067-84127068
allele	-/CT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3320331	chr1:84125858-84127369	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
2	esv3320333	chr1:84126044-84127201	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
3	esv3320330	chr1:84126063-84127162	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3320328	chr1:84126090-84127178	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
5	esv3320332	chr1:84126117-84127120	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv12667	chr1:84126185-84127086	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv3320334	chr1:84126185-84127092	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv1022050	chr1:84127066-84127068	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84122800-84131800	Weak transcription	Pancreas	Pancrea
2	chr1:84126400-84132000	Weak transcription	H9 Derived Neuron Cultured 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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