Variant report

Variant	rs536160399
Chromosome Location	chr6:30430752-30430753
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025667	chr6:30292845-30638066	Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	825 gene(s)	inside rSNPs	diseases
2	esv3519970	chr6:30382942-31378788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
3	esv3519971	chr6:30382942-31378788	Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1030 gene(s)	inside rSNPs	diseases
4	nsv601478	chr6:30383768-30438226	Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	esv3336846	chr6:30420111-30432946	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases
6	nsv601481	chr6:30422632-31284253	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1012 gene(s)	inside rSNPs	diseases
7	nsv884065	chr6:30430520-30446055	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30429800-30430800	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
2	chr6:30429800-30431200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
3	chr6:30429800-30431400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
4	chr6:30429800-30434200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
5	chr6:30430200-30431200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
6	chr6:30430400-30430800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
7	chr6:30430400-30431000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
8	chr6:30430400-30431000	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
9	chr6:30430400-30431200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
10	chr6:30430400-30431200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr6:30430400-30431200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
12	chr6:30430600-30431000	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
13	chr6:30430600-30431000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
14	chr6:30430600-30431200	Bivalent Enhancer	Primary T cells from cord blood	blood
15	chr6:30430600-30431400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
16	chr6:30430600-30431600	Bivalent Enhancer	Primary monocytes fromperipheralblood	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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