Variant report

Variant	rs150387733
Chromosome Location	chr5:92443322-92443323
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	nsv1015770	chr5:91911877-92498264	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv830399	chr5:92290915-92462490	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1029175	chr5:92436038-92548473	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv980987	chr5:92442201-92446772	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:92441800-92444000	Enhancers	Fetal Kidney	kidney
2	chr5:92442200-92444200	Enhancers	Fetal Lung	lung
3	chr5:92442200-92444200	Enhancers	Ovary	ovary
4	chr5:92442800-92443800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr5:92442800-92443800	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr5:92442800-92444200	Enhancers	Adipose Nuclei	Adipose
7	chr5:92443000-92443600	Enhancers	Colon Smooth Muscle	Colon
8	chr5:92443000-92443800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:92443000-92444200	Enhancers	Fetal Stomach	stomach
10	chr5:92443200-92444000	Weak transcription	Stomach Smooth Muscle	stomach

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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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