Variant report

Variant	rs11225421
Chromosome Location	chr11:102654682-102654683
allele	C/T
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	chr11:102651600-102667600	Weak transcription	NHDF-Ad	bronchial
2	chr11:102652000-102656800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr11:102652000-102661200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:102652000-102661200	Weak transcription	NHLF	lung
5	chr11:102652600-102655200	Enhancers	HMEC	breast
6	chr11:102652600-102656800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr11:102653000-102655600	Enhancers	NHEK	skin
8	chr11:102653200-102655000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:102653400-102655200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr11:102654200-102655600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:102654400-102655000	Enhancers	Stomach Mucosa	stomach

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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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