Variant report

Variant	rs2118494
Chromosome Location	chr4:166376077-166376078
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166362200-166381600	Weak transcription	Fetal Stomach	stomach
2	chr4:166362400-166381600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:166362400-166382400	Weak transcription	Aorta	Aorta
4	chr4:166362400-166384600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr4:166362600-166379000	Weak transcription	Fetal Brain Female	brain
6	chr4:166362800-166379200	Weak transcription	Brain Anterior Caudate	brain
7	chr4:166372400-166379000	Weak transcription	Fetal Brain Male	brain
8	chr4:166375000-166376200	Enhancers	HMEC	breast
9	chr4:166375200-166376400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:166375200-166376400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:166376000-166376200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:166376000-166376400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr4:166376000-166382600	Weak transcription	HepG2	liver

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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