Variant report

Variant	rs3923812
Chromosome Location	chr3:133803719-133803720
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133800400-133805200	Weak transcription	Esophagus	oesophagus
2	chr3:133801000-133806800	Enhancers	Placenta	Placenta
3	chr3:133802600-133803800	Weak transcription	Gastric	stomach
4	chr3:133802600-133804400	Enhancers	Placenta Amnion	Placenta Amnion
5	chr3:133802600-133804600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr3:133802600-133804600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr3:133802800-133812000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:133803000-133804600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:133803400-133804200	Enhancers	NHEK	skin
10	chr3:133803400-133804800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:133803600-133803800	Enhancers	HMEC	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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