Variant report

Variant	rs467207
Chromosome Location	chr21:39996082-39996083
allele	A/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	chr21:39989200-39997600	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr21:39993200-39996600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr21:39995200-39999200	Weak transcription	Gastric	stomach
4	chr21:39995200-40002400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr21:39995400-39996600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr21:39995400-39996600	Enhancers	Ovary	ovary
7	chr21:39995600-39996600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr21:39996000-39996200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr21:39996000-39996600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr21:39996000-39996600	Enhancers	Aorta	Aorta
11	chr21:39996000-39996600	Enhancers	Spleen	Spleen

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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