Variant report

Variant rs56096705
Chromosome Location chr1:120145484-120145485
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:120115200-120160800 Weak transcription Gastric stomach
2 chr1:120135200-120151000 Weak transcription Fetal Stomach stomach
3 chr1:120139200-120145600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:120139200-120145600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr1:120139200-120145800 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr1:120139200-120146000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr1:120139400-120146000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr1:120139800-120156600 Weak transcription Left Ventricle heart
9 chr1:120141800-120150600 Weak transcription Placenta Amnion Placenta Amnion
10 chr1:120142400-120146800 Enhancers Fetal Lung lung
11 chr1:120142800-120146400 Enhancers Fetal Intestine Large intestine
12 chr1:120144200-120145800 Weak transcription Ovary ovary
13 chr1:120144600-120146800 Enhancers Primary monocytes fromperipheralblood blood
14 chr1:120145000-120145600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr1:120145000-120145600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:120145000-120146200 Enhancers HUVEC blood vessel
17 chr1:120145200-120146200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
18 chr1:120145200-120146600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
19 chr1:120145200-120147000 Enhancers HMEC breast
20 chr1:120145200-120147600 Weak transcription HepG2 liver
21 chr1:120145200-120148600 Enhancers NHEK skin
22 chr1:120145400-120145600 Enhancers Placenta Placenta
23 chr1:120145400-120146000 Weak transcription Lung lung
24 chr1:120145400-120149200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
25 chr1:120145400-120150800 Weak transcription Fetal Intestine Small intestine

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