Variant report

Variant	rs587700695
Chromosome Location	chr19:41962863-41962864
allele	A/C
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	nsv519523	chr19:41962486-42001210	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1061157	chr19:41962486-42007875	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv510767	chr19:41962486-42049165	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv911770	chr19:41962486-42066279	Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv911771	chr19:41962486-42085873	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr19:41955800-41963000	Weak transcription	Fetal Intestine Large	intestine
2	chr19:41961200-41963800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr19:41962200-41963000	Flanking Active TSS	HUVEC	blood vessel
4	chr19:41962200-41964200	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr19:41962400-41963800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr19:41962400-41964000	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr19:41962400-41964200	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr19:41962400-41964200	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr19:41962600-41963000	Enhancers	Fetal Thymus	thymus
10	chr19:41962600-41963200	Enhancers	Primary T cells fromperipheralblood	blood
11	chr19:41962600-41963600	Flanking Active TSS	GM12878-XiMat	blood
12	chr19:41962600-41964000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr19:41962600-41964000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
14	chr19:41962600-41964200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr19:41962600-41964400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr19:41962800-41964200	Enhancers	Primary T helper memory cells from peripheral blood 1	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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