Variant report

Variant	rs62428160
Chromosome Location	chr6:82714762-82714763
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82706200-82715000	Weak transcription	Placenta	Placenta
2	chr6:82707600-82715200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:82708200-82722400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:82709200-82715200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr6:82709400-82723000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:82711800-82715000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:82713800-82715600	Weak transcription	Right Atrium	heart
8	chr6:82714000-82714800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr6:82714200-82714800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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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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