Variant report

Variant rs13378441
Chromosome Location chr13:52448670-52448671
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:52433800-52479400 Weak transcription HepG2 liver
2 chr13:52438200-52455400 Weak transcription Fetal Intestine Small intestine
3 chr13:52446200-52457000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr13:52447000-52448800 Enhancers HSMMtube muscle
5 chr13:52447800-52448800 Weak transcription Fetal Kidney kidney
6 chr13:52447800-52449000 Enhancers Fetal Thymus thymus
7 chr13:52448000-52450000 Enhancers Cortex derived primary cultured neurospheres brain
8 chr13:52448200-52448800 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr13:52448200-52448800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr13:52448200-52448800 Enhancers Fetal Brain Male brain
11 chr13:52448200-52448800 Enhancers Fetal Brain Female brain
12 chr13:52448200-52449400 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr13:52448200-52457000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr13:52448400-52449000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr13:52448400-52449200 Enhancers Brain Cingulate Gyrus brain
16 chr13:52448600-52448800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
17 chr13:52448600-52449200 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
18 chr13:52448600-52449200 Flanking Active TSS Brain Germinal Matrix brain
19 chr13:52448600-52449400 Enhancers Brain Anterior Caudate brain
20 chr13:52448600-52449600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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