Variant report

Variant	rs12085900
Chromosome Location	chr1:69575293-69575294
allele	A/G
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	chr1:69571400-69575800	Weak transcription	Fetal Brain Male	brain
2	chr1:69572600-69576400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:69575000-69576000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:69575000-69576000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr1:69575000-69576000	Flanking Active TSS	NHEK	skin
6	chr1:69575000-69576200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:69575000-69576800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:69575000-69577000	Enhancers	HMEC	breast
9	chr1:69575200-69575800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr1:69575200-69576000	Enhancers	hESC Derived CD56+ Mesoderm 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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