Variant report

Variant	rs527878359
Chromosome Location	chr7:129231825-129231826
allele	C/T
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	nsv831128	chr7:129063040-129240800	Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	esv3477489	chr7:129230871-129232079	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv3477488	chr7:129230993-129231919	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv3477490	chr7:129231007-129231918	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:129229800-129236000	Enhancers	A549	lung
2	chr7:129231800-129232600	Enhancers	HMEC	breast
3	chr7:129231800-129233800	Enhancers	Placenta	Placenta
4	chr7:129231800-129237000	Enhancers	Osteobl	bone

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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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