Variant report

Variant rs17758796
Chromosome Location chr14:48006091-48006092
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:48000000-48008000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr14:48004400-48008400 Enhancers ES-I3 Cell Line embryonic stem cell
3 chr14:48004600-48007000 Enhancers HUES6 Cell Line embryonic stem cell
4 chr14:48005000-48006400 Enhancers Fetal Brain Female brain
5 chr14:48005000-48008400 Enhancers HUES48 Cell Line embryonic stem cell
6 chr14:48005000-48008400 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr14:48005200-48006400 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr14:48005200-48007600 Enhancers HUES64 Cell Line embryonic stem cell
9 chr14:48005400-48006400 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr14:48005400-48008200 Weak transcription H9 Cell Line embryonic stem cell
11 chr14:48005600-48007200 Enhancers ES-WA7 Cell Line embryonic stem cell
12 chr14:48005800-48018800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr14:48006000-48006200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr14:48006000-48006600 Weak transcription Brain Germinal Matrix brain
15 chr14:48006000-48008200 Weak transcription H1 Cell Line embryonic stem cell

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