Variant report

Variant	rs547565638
Chromosome Location	chr1:158915842-158915843
allele	G/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	nsv1002401	chr1:158712627-158972031	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv3376764	chr1:158761947-158998617	Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv872485	chr1:158863845-158922287	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1007597	chr1:158874806-158934301	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	esv3369957	chr1:158915589-159003393	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158902200-158920000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr1:158905600-158921800	Strong transcription	Primary T cells fromperipheralblood	blood
3	chr1:158905600-158922000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr1:158905800-158930200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr1:158906600-158919600	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr1:158907000-158919200	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:158907200-158918200	Weak transcription	Primary B cells from cord blood	blood
8	chr1:158909200-158921800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:158911000-158922400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr1:158912800-158917600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:158913200-158922200	Strong transcription	Primary T cells from cord blood	blood
12	chr1:158913400-158922800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr1:158913600-158922800	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr1:158914600-158916000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:158915200-158916000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr1:158915200-158916600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr1:158915600-158917200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr1:158915600-158918800	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood

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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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