Variant report

Variant	rs10005876
Chromosome Location	chr4:160332115-160332116
allele	A/G
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	chr4:160323400-160335800	Weak transcription	Left Ventricle	heart
2	chr4:160330400-160332200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:160330600-160332200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:160331000-160332200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr4:160331000-160332200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:160331400-160332400	Enhancers	Fetal Heart	heart
7	chr4:160331600-160332400	Enhancers	HMEC	breast
8	chr4:160331800-160332400	Enhancers	NHEK	skin
9	chr4:160332000-160333800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:160332000-160334000	Weak transcription	NH-A	brain

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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