Variant report

Variant	rs539951741
Chromosome Location	chr10:25978263-25978264
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3360337	chr10:25976571-25979119	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
2	esv3515335	chr10:25976621-25979044	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
3	esv3515336	chr10:25976621-25979044	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
4	esv3356517	chr10:25977096-25978544	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:25962800-25993600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:25978200-25978600	Enhancers	Right Atrium	heart
3	chr10:25978200-25979000	Enhancers	H1 BMP4 Derived Trophoblast 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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