Variant report

Variant	rs75381504
Chromosome Location	chr6:5898978-5898979
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv513296	chr6:5896617-5900093	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
2	esv3472047	chr6:5898314-5898983	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3513838	chr6:5898332-5898987	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv511336	chr6:5898375-5900268	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv4819	chr6:5898415-5899236	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5893200-5899000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:5898200-5899800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:5898200-5900000	Enhancers	NHDF-Ad	bronchial
4	chr6:5898400-5899200	Enhancers	Adipose Nuclei	Adipose
5	chr6:5898600-5899400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:5898800-5899000	Weak transcription	Pancreas	Pancrea

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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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