Variant report

Variant	rs13014294
Chromosome Location	chr2:55142051-55142052
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834069	chr2:55096597-55251680	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55095200-55148200	Weak transcription	Primary B cells from peripheral blood	blood
2	chr2:55134000-55153800	Weak transcription	Brain Angular Gyrus	brain
3	chr2:55134200-55147600	Weak transcription	Fetal Brain Female	brain
4	chr2:55134400-55153600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr2:55136200-55145600	Weak transcription	HepG2	liver
6	chr2:55139800-55142400	Weak transcription	NHLF	lung
7	chr2:55140400-55142600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:55142000-55142200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr2:55142000-55142600	Enhancers	Skeletal Muscle Female	skeletal muscle

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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