Variant report

Variant	rs17714516
Chromosome Location	chr8:91580379-91580380
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91571000-91584600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:91573800-91581000	Weak transcription	Hela-S3	cervix
3	chr8:91576800-91580400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr8:91576800-91580400	Weak transcription	HMEC	breast
5	chr8:91576800-91580600	Weak transcription	NHEK	skin
6	chr8:91580200-91580400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:91580200-91580400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:91580200-91581200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr8:91580200-91581400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:91580200-91582400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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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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