Variant report

Variant	rs35673063
Chromosome Location	chr8:130530396-130530397
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130526800-130531800	Strong transcription	K562	blood
2	chr8:130527400-130530600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:130528800-130532600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr8:130529000-130531000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr8:130529000-130532800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr8:130529200-130530800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr8:130529200-130538400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:130530000-130530400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr8:130530000-130530600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr8:130530000-130530600	Genic enhancers	Dnd41	blood
11	chr8:130530000-130530800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	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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