Variant report

Variant rs10151487
Chromosome Location chr14:67369566-67369567
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67356000-67371000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr14:67356200-67377600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr14:67357600-67369800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr14:67360200-67372800 Weak transcription Pancreas Pancrea
5 chr14:67360200-67382800 Weak transcription Left Ventricle heart

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