Variant report

Variant	rs7715385
Chromosome Location	chr5:167494376-167494377
allele	A/G
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	chr5:167468000-167500800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:167483200-167502400	Weak transcription	Fetal Heart	heart
3	chr5:167488400-167496800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr5:167491600-167494800	Weak transcription	Right Ventricle	heart
5	chr5:167491800-167494600	Weak transcription	Left Ventricle	heart
6	chr5:167491800-167500600	Weak transcription	HSMM	muscle
7	chr5:167491800-167509200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:167492000-167494600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:167492000-167500600	Weak transcription	NH-A	brain
10	chr5:167492800-167497400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr5:167494000-167495000	Weak transcription	NHEK	skin
12	chr5:167494000-167495400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
13	chr5:167494200-167498000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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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