Variant report

Variant	rs567891847
Chromosome Location	chr9:72217342-72217343
allele	C/T
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	nsv893437	chr9:72118962-72223176	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3425590	chr9:72217232-72221730	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72207800-72220200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr9:72208600-72217400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr9:72209200-72219600	Weak transcription	Gastric	stomach
4	chr9:72209800-72217600	Weak transcription	Fetal Lung	lung
5	chr9:72212000-72219200	Weak transcription	Liver	Liver
6	chr9:72214400-72217600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr9:72215000-72219600	Weak transcription	Right Ventricle	heart
8	chr9:72215000-72220200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:72215200-72219600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr9:72215200-72221000	Weak transcription	Right Atrium	heart
11	chr9:72215400-72217600	Weak transcription	Fetal Muscle Leg	muscle
12	chr9:72215400-72217800	Weak transcription	Fetal Heart	heart
13	chr9:72215400-72219200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr9:72215600-72235200	Weak transcription	Aorta	Aorta
15	chr9:72215800-72218400	Enhancers	HUVEC	blood vessel
16	chr9:72216600-72217600	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr9:72217000-72217400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr9:72217200-72217400	Enhancers	Pancreas	Pancrea
19	chr9:72217200-72221200	Enhancers	Ovary	ovary

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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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