Variant report

Variant	rs9885797
Chromosome Location	chr6:149065393-149065394
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149057200-149067000	Weak transcription	Primary B cells from cord blood	blood
2	chr6:149058800-149067000	Weak transcription	Aorta	Aorta
3	chr6:149062400-149067000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:149063600-149067000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr6:149064000-149066200	Enhancers	Pancreas	Pancrea
6	chr6:149064600-149066400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr6:149064800-149065400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:149064800-149065400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr6:149065000-149067400	Weak transcription	Gastric	stomach
10	chr6:149065200-149065400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr6:149065200-149066800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr6:149065200-149067000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:149065200-149067400	Weak transcription	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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