Variant report

Variant	rs7680580
Chromosome Location	chr4:81232795-81232796
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81231000-81235000	Enhancers	NHDF-Ad	bronchial
2	chr4:81231400-81234000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:81231400-81235800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:81231400-81239200	Weak transcription	HSMM	muscle
5	chr4:81231600-81243400	Weak transcription	NH-A	brain
6	chr4:81231800-81233800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr4:81231800-81234200	Weak transcription	Osteobl	bone
8	chr4:81232000-81232800	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr4:81232000-81234200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:81232200-81242200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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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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