Variant report

Variant	rs368042915
Chromosome Location	chr4:47124884-47124885
allele	A/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	nsv537078	chr4:47059778-47137372	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv829922	chr4:47093785-47261181	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv879003	chr4:47102993-47215939	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv3377198	chr4:47124595-47126943	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:47124400-47125000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr4:47124600-47125000	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr4:47124600-47125200	Enhancers	Adipose Nuclei	Adipose
4	chr4:47124600-47125200	Enhancers	Brain Angular Gyrus	brain
5	chr4:47124600-47125200	Enhancers	Brain Cingulate Gyrus	brain
6	chr4:47124600-47125200	Enhancers	Brain Hippocampus Middle	brain
7	chr4:47124600-47125200	Enhancers	Fetal Intestine Small	intestine
8	chr4:47124600-47125200	Enhancers	Fetal Lung	lung
9	chr4:47124800-47125000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:47124800-47125200	Enhancers	Liver	Liver
11	chr4:47124800-47125200	Enhancers	Brain Substantia Nigra	brain
12	chr4:47124800-47125200	Enhancers	Fetal Kidney	kidney

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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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