Variant report

Variant	rs7750798
Chromosome Location	chr6:107295341-107295342
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	chr6:107257600-107297000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:107292600-107295600	Enhancers	Primary B cells from peripheral blood	blood
3	chr6:107292600-107297000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr6:107293200-107299800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr6:107294200-107295400	Flanking Active TSS	GM12878-XiMat	blood
6	chr6:107294800-107295400	Flanking Active TSS	K562	blood
7	chr6:107295000-107295400	Enhancers	Fetal Brain Male	brain
8	chr6:107295000-107295800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr6:107295200-107295400	Enhancers	Primary hematopoietic stem cells	blood
10	chr6:107295200-107295800	Enhancers	Primary B cells from cord blood	blood
11	chr6:107295200-107299800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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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