Variant report

Variant	rs57234842
Chromosome Location	chr4:160332870-160332871
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:160323400-160335800	Weak transcription	Left Ventricle	heart
2	chr4:160332000-160333800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:160332000-160334000	Weak transcription	NH-A	brain
4	chr4:160332200-160334400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:160332200-160337400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:160332200-160337400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr4:160332400-160337400	Weak transcription	NHEK	skin
8	chr4:160332400-160338400	Weak transcription	HMEC	breast

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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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