Variant report

Variant	rs7117397
Chromosome Location	chr11:76560978-76560979
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:76549600-76561000	Weak transcription	Right Atrium	heart
2	chr11:76549600-76570800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:76549800-76572000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:76550600-76566400	Weak transcription	Lung	lung
5	chr11:76556400-76561600	Weak transcription	Liver	Liver
6	chr11:76558800-76561600	Weak transcription	Adipose Nuclei	Adipose
7	chr11:76559000-76561200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:76559000-76561400	Weak transcription	Ovary	ovary
9	chr11:76559200-76561800	Weak transcription	Placenta	Placenta
10	chr11:76559600-76562000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:76560200-76562400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:76560400-76562000	Enhancers	K562	blood
13	chr11:76560400-76562200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr11:76560400-76562200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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