Variant report

Variant	rs74094997
Chromosome Location	chr1:84476830-84476831
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84474000-84484000	Weak transcription	Esophagus	oesophagus
2	chr1:84474600-84477600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:84475000-84477000	Weak transcription	HMEC	breast
4	chr1:84475000-84477600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr1:84475200-84477200	Weak transcription	NHEK	skin
6	chr1:84475400-84477000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:84475400-84477200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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