Variant report

Variant rs13353796
Chromosome Location chr4:54502657-54502658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:54485200-54505800 Weak transcription Esophagus oesophagus
2 chr4:54494600-54507000 Weak transcription Right Ventricle heart
3 chr4:54499200-54503000 Enhancers Ovary ovary
4 chr4:54501200-54502800 Enhancers Pancreas Pancrea
5 chr4:54501200-54503000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr4:54501400-54503000 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr4:54501400-54506400 Weak transcription Stomach Mucosa stomach
8 chr4:54501400-54507000 Weak transcription Left Ventricle heart
9 chr4:54501400-54507000 Weak transcription Lung lung
10 chr4:54501400-54510800 Weak transcription Right Atrium heart
11 chr4:54501600-54507000 Weak transcription Fetal Intestine Large intestine
12 chr4:54501800-54503400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr4:54502000-54502800 Enhancers Cortex derived primary cultured neurospheres brain
14 chr4:54502000-54502800 Enhancers Brain Hippocampus Middle brain
15 chr4:54502000-54502800 Enhancers Brain Substantia Nigra brain
16 chr4:54502200-54502800 Enhancers Adipose Nuclei Adipose
17 chr4:54502200-54506600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr4:54502200-54507000 Weak transcription Gastric stomach
19 chr4:54502400-54502800 Enhancers GM12878-XiMat blood
20 chr4:54502600-54502800 Bivalent Enhancer Fetal Lung lung

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