Variant report

Variant rs72902655
Chromosome Location chr2:189591372-189591373
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:189586400-189591400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
2 chr2:189588000-189592800 Weak transcription Fetal Lung lung
3 chr2:189590200-189592800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr2:189590400-189593000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr2:189590600-189591600 Enhancers HSMM muscle
6 chr2:189590600-189592400 Enhancers NH-A brain
7 chr2:189590800-189591400 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr2:189590800-189592200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr2:189590800-189592400 Enhancers NHEK skin
10 chr2:189591200-189591800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr2:189591200-189591800 Enhancers NHDF-Ad bronchial
12 chr2:189591200-189592200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr2:189591200-189592400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr2:189591200-189592400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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