Variant report

Variant rs12152385
Chromosome Location chr3:21696139-21696140
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:21683800-21706600 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr3:21685600-21707200 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr3:21687200-21696400 Weak transcription Aorta Aorta
4 chr3:21687200-21701800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr3:21687200-21706200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr3:21687200-21709600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr3:21687400-21706800 Weak transcription Fetal Lung lung
8 chr3:21688000-21699000 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr3:21688000-21707000 Weak transcription Fetal Muscle Leg muscle
10 chr3:21695000-21703600 Weak transcription K562 blood
11 chr3:21695800-21696200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr3:21695800-21696400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr3:21695800-21696800 Enhancers NHDF-Ad bronchial
14 chr3:21695800-21696800 Enhancers NHLF lung
15 chr3:21695800-21697000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr3:21695800-21697000 Enhancers Muscle Satellite Cultured Cells --
17 chr3:21696000-21696200 Flanking Active TSS NH-A brain
18 chr3:21696000-21696600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
19 chr3:21696000-21696600 Enhancers Placenta Amnion Placenta Amnion
20 chr3:21696000-21696800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
21 chr3:21696000-21696800 Enhancers HSMM muscle

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