Variant report

Variant	rs57471700
Chromosome Location	chr13:50434728-50434729
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	chr13:50422200-50436600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr13:50432400-50435400	Enhancers	Placenta	Placenta
3	chr13:50433400-50435000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr13:50433800-50435000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr13:50434000-50438200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:50434200-50442000	Weak transcription	Pancreas	Pancrea
7	chr13:50434600-50435000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr13:50434600-50435400	Enhancers	A549	lung

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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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