Variant report

Variant	rs532645117
Chromosome Location	chr9:108520848-108520849
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	nsv893693	chr9:108427062-108683134	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv615116	chr9:108468129-108546438	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	nsv893694	chr9:108486533-108854018	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv982335	chr9:108520769-108531325	Strong transcription Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108513800-108521400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr9:108514000-108540000	Weak transcription	HSMMtube	muscle
3	chr9:108514800-108521400	Weak transcription	Spleen	Spleen
4	chr9:108515200-108521000	Weak transcription	Dnd41	blood
5	chr9:108515200-108522800	Weak transcription	Left Ventricle	heart
6	chr9:108515200-108545000	Weak transcription	K562	blood
7	chr9:108515200-108560600	Weak transcription	Ovary	ovary
8	chr9:108515400-108523400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:108515400-108536800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:108515600-108522400	Weak transcription	Liver	Liver
11	chr9:108515600-108538600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:108517200-108522000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr9:108517800-108538400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:108519200-108521000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr9:108520200-108521000	Strong transcription	Primary B cells from cord blood	blood
16	chr9:108520600-108522800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr9:108520600-108523200	Weak transcription	Pancreas	Pancrea
18	chr9:108520600-108535200	Weak transcription	Primary hematopoietic stem cells	blood
19	chr9:108520600-108546400	Weak transcription	Fetal Intestine Small	intestine

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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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