Variant report

Variant	rs1543862
Chromosome Location	chr2:72235898-72235899
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	chr2:72232600-72240600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:72233800-72237600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:72235200-72236200	Enhancers	Placenta Amnion	Placenta Amnion
4	chr2:72235400-72236000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:72235400-72236200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:72235400-72236200	Enhancers	NHEK	skin
7	chr2:72235400-72236400	Enhancers	Hela-S3	cervix
8	chr2:72235400-72237400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr2:72235600-72236000	Enhancers	Esophagus	oesophagus
10	chr2:72235600-72236800	Enhancers	Fetal Muscle Trunk	muscle
11	chr2:72235800-72236200	Enhancers	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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