Variant report

Variant rs574437207
Chromosome Location chr14:32773603-32773604
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32768000-32780000 Weak transcription Psoas Muscle Psoas
2 chr14:32768600-32776600 Weak transcription Colon Smooth Muscle Colon
3 chr14:32769800-32777200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr14:32769800-32780800 Weak transcription Left Ventricle heart
5 chr14:32772200-32774000 Enhancers Liver Liver
6 chr14:32772400-32774000 Enhancers Fetal Intestine Small intestine
7 chr14:32772800-32773800 Enhancers HepG2 liver
8 chr14:32772800-32778400 Enhancers Fetal Intestine Large intestine
9 chr14:32773000-32773800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr14:32773200-32774000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr14:32773200-32774000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
12 chr14:32773200-32774000 Enhancers Brain Hippocampus Middle brain
13 chr14:32773400-32773800 Active TSS Pancreatic Islets Pancreatic Islet
14 chr14:32773400-32774000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
15 chr14:32773600-32773800 Enhancers Esophagus oesophagus
16 chr14:32773600-32774000 Enhancers Pancreas Pancrea
17 chr14:32773600-32774400 Enhancers Brain Cingulate Gyrus brain
18 chr14:32773600-32774400 Enhancers Brain Inferior Temporal Lobe brain
19 chr14:32773600-32774400 Enhancers Brain Substantia Nigra brain
20 chr14:32773600-32776800 Weak transcription Fetal Heart heart

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