Variant report

Variant	rs80051601
Chromosome Location	chr9:95439713-95439714
allele	C/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	nsv972419	chr9:95438927-95440430	Weak transcription Enhancers ZNF genes & repeats	TF binding region Chromatin interactive 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	chr9:95433400-95442800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:95433800-95441800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:95433800-95444000	Weak transcription	Fetal Brain Female	brain
4	chr9:95434000-95439800	Weak transcription	Brain Germinal Matrix	brain
5	chr9:95434000-95441800	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr9:95434000-95441800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:95434000-95442400	Weak transcription	NHDF-Ad	bronchial
8	chr9:95434200-95441800	Weak transcription	Esophagus	oesophagus
9	chr9:95434200-95441800	Weak transcription	NHEK	skin
10	chr9:95434200-95442800	Weak transcription	Placenta	Placenta
11	chr9:95439000-95440800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr9:95439200-95439800	Enhancers	Fetal Thymus	thymus
13	chr9:95439600-95439800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr9:95439600-95442200	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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