Variant report
Variant | rs35374718 |
---|---|
Chromosome Location | chr11:26351609-26351610 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:26341800-26353200 | Weak transcription | Pancreas | Pancrea |
2 | chr11:26349800-26351800 | Enhancers | Fetal Brain Male | brain |
3 | chr11:26349800-26353200 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
4 | chr11:26350000-26352000 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
5 | chr11:26350000-26353200 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
6 | chr11:26350000-26353200 | Enhancers | hESC Derived CD56+ Ectoderm Cultured Cells | ES cell derived |
7 | chr11:26350200-26352000 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
8 | chr11:26350400-26352000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
9 | chr11:26350600-26351800 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
10 | chr11:26350800-26351800 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
11 | chr11:26351200-26353200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
12 | chr11:26351400-26353400 | Weak transcription | Spleen | Spleen |