Variant report

Variant rs17055994
Chromosome Location chr13:38109185-38109186
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:38105600-38115000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr13:38106800-38109200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr13:38107400-38109200 Enhancers Osteobl bone
4 chr13:38108000-38109200 Enhancers NH-A brain
5 chr13:38108400-38109200 Flanking Active TSS NHDF-Ad bronchial
6 chr13:38108600-38109200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr13:38108600-38109200 Flanking Active TSS Muscle Satellite Cultured Cells --
8 chr13:38108600-38109200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr13:38108800-38109200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr13:38108800-38112600 Weak transcription Fetal Lung lung
11 chr13:38108800-38113400 Weak transcription NHLF lung
12 chr13:38109000-38110600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow

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