Variant report

Variant	rs60988778
Chromosome Location	chr12:65377773-65377774
allele	C/T
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	chr12:65376200-65384600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr12:65376400-65383600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:65377400-65378200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr12:65377400-65378400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:65377400-65378400	Enhancers	HMEC	breast
6	chr12:65377400-65378400	Enhancers	NHEK	skin
7	chr12:65377600-65378200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:65377600-65378200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr12:65377600-65378800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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