Variant report

Variant	rs576302396
Chromosome Location	chr6:144453735-144453736
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3449955	chr6:144452509-144454707	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv2426838	chr6:144452778-144454341	Enhancers Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases
3	esv3501887	chr6:144453229-144453854	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
4	esv3501888	chr6:144453229-144453854	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
5	esv3443680	chr6:144453289-144453786	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3440965	chr6:144453292-144453764	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144451200-144460400	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr6:144452400-144456200	Weak transcription	NHLF	lung
3	chr6:144453000-144454600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:144453000-144455200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:144453000-144455200	Weak transcription	NHDF-Ad	bronchial
6	chr6:144453000-144455200	Weak transcription	Osteobl	bone
7	chr6:144453000-144458800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:144453200-144455200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr6:144453200-144455400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:144453600-144456200	Enhancers	HUVEC	blood vessel

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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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