Variant report

Variant rs11569132
Chromosome Location chr4:110930676-110930677
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:110907000-110932400 Weak transcription Psoas Muscle Psoas
2 chr4:110910400-110935200 Weak transcription Pancreas Pancrea
3 chr4:110919000-110935200 Weak transcription Left Ventricle heart
4 chr4:110920800-110935800 Strong transcription Skeletal Muscle Female skeletal muscle
5 chr4:110926800-110931200 Enhancers Liver Liver
6 chr4:110927400-110931000 Strong transcription Skeletal Muscle Male skeletal muscle
7 chr4:110928400-110931400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr4:110928400-110931400 Enhancers Fetal Intestine Large intestine
9 chr4:110930000-110930800 Weak transcription Fetal Kidney kidney
10 chr4:110930000-110937200 Weak transcription Fetal Intestine Small intestine
11 chr4:110930200-110932400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr4:110930400-110941600 Weak transcription Fetal Heart heart
13 chr4:110930600-110930800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr4:110930600-110931000 Enhancers HUES6 Cell Line embryonic stem cell
15 chr4:110930600-110931000 Enhancers Cortex derived primary cultured neurospheres brain
16 chr4:110930600-110931000 Enhancers Brain Germinal Matrix brain

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