Variant report

Variant	rs1794739
Chromosome Location	chr12:120856214-120856215
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:120827200-120875200	Weak transcription	Right Atrium	heart
2	chr12:120852400-120875200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:120854200-120857200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:120855600-120856400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:120855800-120856400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr12:120855800-120856400	Enhancers	HMEC	breast
7	chr12:120855800-120856400	Enhancers	NHEK	skin
8	chr12:120855800-120856800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:120856000-120856800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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