Variant report

Variant rs587683853
Chromosome Location chr1:120142854-120142855
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:120115200-120160800 Weak transcription Gastric stomach
2 chr1:120133600-120144800 Weak transcription Placenta Placenta
3 chr1:120135200-120151000 Weak transcription Fetal Stomach stomach
4 chr1:120139000-120145000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:120139000-120145200 Weak transcription NHEK skin
6 chr1:120139200-120145600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:120139200-120145600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr1:120139200-120145800 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr1:120139200-120146000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr1:120139400-120146000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr1:120139800-120156600 Weak transcription Left Ventricle heart
12 chr1:120141800-120150600 Weak transcription Placenta Amnion Placenta Amnion
13 chr1:120142400-120146800 Enhancers Fetal Lung lung
14 chr1:120142800-120143400 Enhancers Fetal Intestine Small intestine
15 chr1:120142800-120146400 Enhancers Fetal Intestine Large intestine

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