Variant report

Variant	rs570595018
Chromosome Location	chr1:66987151-66987152
allele	A/T
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	nsv518465	chr1:66986377-66988586	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:66983600-66987200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:66985800-66988000	Enhancers	A549	lung
3	chr1:66986000-66987200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:66986000-66987200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr1:66986200-66989400	Weak transcription	HepG2	liver
6	chr1:66987000-66987200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:66987000-66987200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:66987000-66988000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr1:66987000-66988200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr1:66987000-66988200	Enhancers	NHLF	lung
11	chr1:66987000-66988400	Enhancers	Osteobl	bone
12	chr1:66987000-66990400	Enhancers	Hela-S3	cervix

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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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