Variant report

Variant	rs73442444
Chromosome Location	chr21:39995856-39995857
allele	C/T
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	chr21:39989200-39997600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr21:39993200-39996600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr21:39994600-39996000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr21:39994600-39996000	Weak transcription	Aorta	Aorta
5	chr21:39994800-39996000	Weak transcription	Spleen	Spleen
6	chr21:39995200-39996000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr21:39995200-39999200	Weak transcription	Gastric	stomach
8	chr21:39995200-40002400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr21:39995400-39996600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr21:39995400-39996600	Enhancers	Ovary	ovary
11	chr21:39995600-39996600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

Quick Search:

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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