Variant report

Variant rs72851132
Chromosome Location chr2:133308754-133308755
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133302400-133321600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:133307000-133313400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr2:133307400-133308800 Enhancers Fetal Brain Male brain
4 chr2:133307400-133309000 Enhancers Fetal Stomach stomach
5 chr2:133307600-133308800 Enhancers Colon Smooth Muscle Colon
6 chr2:133307600-133308800 Enhancers Duodenum Smooth Muscle Duodenum
7 chr2:133307600-133308800 Enhancers Fetal Lung lung
8 chr2:133307800-133308800 Enhancers Rectal Smooth Muscle rectum
9 chr2:133307800-133309000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr2:133307800-133309000 Enhancers NHDF-Ad bronchial
11 chr2:133307800-133309400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr2:133308000-133308800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr2:133308200-133308800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
14 chr2:133308400-133308800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr2:133308400-133309200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr2:133308600-133308800 Enhancers Fetal Heart heart

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