Variant report

Variant rs10458387
Chromosome Location chr1:162093507-162093508
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:162085800-162098600 Weak transcription HepG2 liver
2 chr1:162087600-162095400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr1:162089600-162098600 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr1:162089600-162098600 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr1:162089800-162098800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr1:162090800-162098800 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr1:162091400-162098600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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