Variant report

Variant	rs190144574
Chromosome Location	chr8:62892767-62892768
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024432	chr8:62086247-62898782	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv932198	chr8:62336705-62914562	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv831338	chr8:62736394-62913048	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv890951	chr8:62889169-62989464	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	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	chr8:62892000-62893000	Enhancers	A549	lung
2	chr8:62892000-62893200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr8:62892000-62893400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr8:62892000-62893400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:62892200-62893200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr8:62892200-62893400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr8:62892400-62893400	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:62892600-62893000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr8:62892600-62893200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr8:62892600-62893200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr8:62892600-62893200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr8:62892600-62893400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr8:62892600-62893800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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