Variant report

Variant	rs17860996
Chromosome Location	chr11:102642753-102642754
allele	A/T
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	chr11:102635400-102647000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr11:102636200-102644200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:102641000-102647200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:102641200-102644200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr11:102641400-102644200	Weak transcription	NHEK	skin
6	chr11:102641600-102643800	Enhancers	HUVEC	blood vessel
7	chr11:102642200-102642800	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr11:102642200-102642800	Enhancers	Stomach Mucosa	stomach
9	chr11:102642400-102644200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:102642400-102644200	Weak transcription	Placenta Amnion	Placenta Amnion

Quick Search:

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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