Variant report

Variant	rs62404281
Chromosome Location	chr6:71848709-71848710
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	chr6:71834600-71848800	Weak transcription	NH-A	brain
2	chr6:71847800-71849800	Enhancers	HMEC	breast
3	chr6:71848200-71849600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:71848200-71849600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr6:71848400-71849400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:71848400-71849600	Enhancers	NHEK	skin
7	chr6:71848600-71849600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:71848600-71849600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:71848600-71849800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr6:71848600-71849800	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr6:71848600-71849800	Enhancers	HSMM	muscle

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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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