Variant report

Variant rs9596712
Chromosome Location chr13:53468175-53468176
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:53461600-53471200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr13:53463000-53471200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr13:53466000-53468400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr13:53466400-53471000 Weak transcription ES-I3 Cell Line embryonic stem cell
5 chr13:53466800-53471000 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr13:53466800-53471200 Weak transcription H9 Cell Line embryonic stem cell
7 chr13:53466800-53472400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr13:53467000-53469600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr13:53467000-53471000 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr13:53467200-53471000 Weak transcription Fetal Brain Female brain
11 chr13:53467400-53469800 Weak transcription Fetal Stomach stomach
12 chr13:53467400-53471000 Weak transcription Cortex derived primary cultured neurospheres brain
13 chr13:53467600-53468200 Enhancers HUES64 Cell Line embryonic stem cell
14 chr13:53468000-53468200 Enhancers Fetal Muscle Leg muscle
15 chr13:53468000-53469000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr13:53468000-53469200 Enhancers Fetal Brain Male brain

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