Variant report

Variant	rs574608154
Chromosome Location	chr3:16996031-16996032
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	nsv980048	chr3:16995372-17016178	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:16984200-17003400	Weak transcription	Spleen	Spleen
2	chr3:16985000-17003400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
3	chr3:16985600-17000400	Weak transcription	Primary T cells from cord blood	blood
4	chr3:16986600-17000400	Weak transcription	Left Ventricle	heart
5	chr3:16986800-17003000	Weak transcription	Ovary	ovary
6	chr3:16987400-17005000	Weak transcription	Primary B cells from cord blood	blood
7	chr3:16987400-17015600	Weak transcription	Aorta	Aorta
8	chr3:16993400-16999600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr3:16993400-17003400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr3:16993400-17005200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr3:16993600-16999600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr3:16993800-17000200	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr3:16993800-17002200	Weak transcription	Primary T helper cells PMA-I stimulated	--

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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