Variant report

Variant	rs142611430
Chromosome Location	chr2:191424741-191424742
allele	A/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	nsv527324	chr2:191423989-191427736	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191411000-191443000	Weak transcription	Right Atrium	heart
2	chr2:191417600-191427800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:191418000-191427000	Weak transcription	Pancreas	Pancrea
4	chr2:191418200-191426800	Weak transcription	Primary T cells from cord blood	blood
5	chr2:191419600-191426800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr2:191419600-191427400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:191424400-191424800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr2:191424400-191424800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr2:191424600-191424800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:191424600-191424800	Enhancers	Left Ventricle	heart
11	chr2:191424600-191426000	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr2:191424600-191427000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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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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