Variant report

Variant	rs60401194
Chromosome Location	chr14:71101397-71101398
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71092200-71107600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr14:71092200-71107600	Weak transcription	HSMM	muscle
3	chr14:71094600-71107200	Weak transcription	HSMMtube	muscle
4	chr14:71097000-71101400	Weak transcription	GM12878-XiMat	blood
5	chr14:71098400-71107200	Weak transcription	Thymus	Thymus
6	chr14:71099000-71101800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:71099000-71107000	Weak transcription	Skeletal Muscle Female	skeletal muscle
8	chr14:71100400-71101800	Strong transcription	Primary B cells from cord blood	blood
9	chr14:71101000-71102000	ZNF genes & repeats	Esophagus	oesophagus
10	chr14:71101000-71103000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr14:71101200-71101600	Strong transcription	Primary B cells from peripheral blood	blood
12	chr14:71101200-71101800	Weak transcription	Fetal Brain Female	brain

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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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