Variant report

Variant	rs10071057
Chromosome Location	chr5:151286475-151286476
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:151284400-151286600	Enhancers	Fetal Lung	lung
2	chr5:151285000-151286600	Enhancers	HSMMtube	muscle
3	chr5:151285200-151286600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr5:151285600-151289000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr5:151285800-151286600	Enhancers	Aorta	Aorta
6	chr5:151285800-151286600	Enhancers	HSMM	muscle
7	chr5:151286000-151290200	Weak transcription	NHEK	skin
8	chr5:151286000-151290600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr5:151286200-151290200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr5:151286400-151286600	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
11	chr5:151286400-151289400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:151286400-151290200	Weak transcription	HMEC	breast

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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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