Variant report

Variant	rs191610150
Chromosome Location	chr1:56400953-56400954
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1818340	chr1:56359741-56408597	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3374566	chr1:56400589-56402612	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
3	esv2614647	chr1:56400766-56402350	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56397200-56403400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr1:56398000-56403400	Weak transcription	Ovary	ovary
3	chr1:56398400-56404000	Weak transcription	Fetal Lung	lung
4	chr1:56398600-56403600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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