Variant report

Variant	rs181982
Chromosome Location	chr6:82485151-82485152
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	chr6:82474200-82485800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:82477600-82485400	Weak transcription	Placenta	Placenta
3	chr6:82480400-82485800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:82483000-82487400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:82483000-82487400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:82483000-82497400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:82483200-82485600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr6:82483600-82485600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr6:82483800-82485200	Enhancers	Liver	Liver
10	chr6:82483800-82485800	Weak transcription	Hela-S3	cervix
11	chr6:82484400-82488400	Enhancers	HepG2	liver

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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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