Variant report

Variant	rs376966582
Chromosome Location	chr5:124450448-124450449
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830475	chr5:124387292-124550256	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv3380266	chr5:124450441-124450783	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:124445800-124455800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr5:124448200-124450800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr5:124448200-124453000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr5:124448200-124453000	Weak transcription	NHLF	lung
5	chr5:124448400-124453400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr5:124449200-124454000	Weak transcription	Dnd41	blood
7	chr5:124449600-124450800	Weak transcription	HSMM	muscle
8	chr5:124449800-124450800	Weak transcription	NHDF-Ad	bronchial
9	chr5:124450200-124451400	Enhancers	Liver	Liver

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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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