Variant report

Variant rs538400859
Chromosome Location chr4:187902336-187902337
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187901200-187902600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr4:187901200-187902600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr4:187901400-187902400 Enhancers HUES64 Cell Line embryonic stem cell
4 chr4:187901400-187902400 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr4:187901400-187902600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
6 chr4:187901400-187902600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
7 chr4:187901400-187902800 Enhancers Cortex derived primary cultured neurospheres brain
8 chr4:187901600-187902600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr4:187901800-187902400 Enhancers Fetal Lung lung
10 chr4:187901800-187905000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr4:187902000-187902400 Enhancers HUES6 Cell Line embryonic stem cell
12 chr4:187902000-187902400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr4:187902200-187902400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr4:187902200-187902600 Enhancers Osteobl bone

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