Variant report

Variant rs1860358
Chromosome Location chr12:564807-564808
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:560400-568200 Weak transcription Gastric stomach
2 chr12:560600-568400 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr12:562400-567200 Weak transcription Stomach Mucosa stomach
4 chr12:563000-568400 Weak transcription Pancreas Pancrea
5 chr12:563200-565000 Weak transcription Left Ventricle heart
6 chr12:563200-568600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr12:563200-568600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr12:563200-568600 Weak transcription Right Ventricle heart
9 chr12:563400-568200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr12:563800-565600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr12:564200-568400 Weak transcription Esophagus oesophagus
12 chr12:564400-565400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr12:564600-565000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr12:564800-565000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr12:564800-565000 Flanking Active TSS Fetal Heart heart

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