Variant report

Variant	rs9450791
Chromosome Location	chr6:88456086-88456087
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	chr6:88452800-88457000	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr6:88452800-88457000	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr6:88453200-88457200	Weak transcription	Primary B cells from cord blood	blood
4	chr6:88453600-88457000	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr6:88453600-88457200	Weak transcription	Primary B cells from peripheral blood	blood
6	chr6:88453800-88457400	Weak transcription	GM12878-XiMat	blood
7	chr6:88455000-88458200	Enhancers	HepG2	liver
8	chr6:88455200-88456600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr6:88455400-88456400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:88456000-88456200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:88456000-88456400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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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