Variant report

Variant rs542918931
Chromosome Location chr14:32773477-32773478
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32765200-32773600 Weak transcription Pancreas Pancrea
2 chr14:32768000-32780000 Weak transcription Psoas Muscle Psoas
3 chr14:32768600-32776600 Weak transcription Colon Smooth Muscle Colon
4 chr14:32769800-32777200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr14:32769800-32780800 Weak transcription Left Ventricle heart
6 chr14:32772200-32774000 Enhancers Liver Liver
7 chr14:32772400-32774000 Enhancers Fetal Intestine Small intestine
8 chr14:32772800-32773600 Enhancers Fetal Heart heart
9 chr14:32772800-32773800 Enhancers HepG2 liver
10 chr14:32772800-32778400 Enhancers Fetal Intestine Large intestine
11 chr14:32773000-32773800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr14:32773200-32774000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr14:32773200-32774000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr14:32773200-32774000 Enhancers Brain Hippocampus Middle brain
15 chr14:32773400-32773800 Active TSS Pancreatic Islets Pancreatic Islet
16 chr14:32773400-32774000 Enhancers Brain Dorsolateral Prefrontal Cortex brain

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