Variant report

Variant	rs373139917
Chromosome Location	chr1:67079072-67079073
allele	A/G
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	nsv1221	chr1:67047908-67092696	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv160302	chr1:67079017-67080809	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:67058000-67092200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:67065800-67082800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr1:67066200-67083800	Weak transcription	NHLF	lung
4	chr1:67066400-67089600	Weak transcription	Brain Angular Gyrus	brain
5	chr1:67068000-67082600	Weak transcription	NHDF-Ad	bronchial
6	chr1:67071600-67094800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:67074000-67081200	Weak transcription	Brain Anterior Caudate	brain
8	chr1:67075400-67079400	Weak transcription	Fetal Heart	heart
9	chr1:67077400-67081000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:67078000-67081600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:67078000-67088400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:67078800-67079200	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:67079000-67079200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr1:67079000-67079200	Enhancers	Aorta	Aorta

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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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