Variant report

Variant rs397801318
Chromosome Location chr2:133279275-133279276
allele -/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133262000-133280400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:133268200-133282800 Weak transcription Fetal Intestine Small intestine
3 chr2:133274400-133280200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr2:133274400-133283200 Weak transcription Pancreas Pancrea
5 chr2:133278400-133280800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:133278600-133279400 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr2:133278600-133279600 Enhancers HMEC breast
8 chr2:133278600-133280600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:133278600-133281000 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr2:133278800-133279400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr2:133278800-133280400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr2:133279000-133280800 Enhancers Brain Germinal Matrix brain
13 chr2:133279000-133282600 Enhancers Fetal Brain Male brain
14 chr2:133279200-133280200 Weak transcription Fetal Brain Female brain
15 chr2:133279200-133280200 Weak transcription NHEK skin
16 chr2:133279200-133281600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr2:133279200-133283000 Weak transcription Fetal Heart heart

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