Variant report

Variant rs376007149
Chromosome Location chr13:63982439-63982440
allele -/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:63978800-63982600 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr13:63981000-63982600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr13:63981800-63982600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr13:63982000-63984000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr13:63982200-63983600 Enhancers HUES64 Cell Line embryonic stem cell
6 chr13:63982400-63982600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr13:63982400-63982600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
8 chr13:63982400-63982600 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr13:63982400-63983000 Enhancers HUES6 Cell Line embryonic stem cell
10 chr13:63982400-63983000 Enhancers Fetal Lung lung
11 chr13:63982400-63983200 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr13:63982400-63983200 Enhancers Rectal Smooth Muscle rectum
13 chr13:63982400-63983400 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr13:63982400-63983600 Enhancers Osteobl bone
15 chr13:63982400-63983800 Active TSS Fetal Brain Male brain

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