Variant report

Variant rs10487783
Chromosome Location chr7:14879871-14879872
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:14873400-14881200 Weak transcription NHLF lung
2 chr7:14875400-14886200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr7:14877000-14880400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr7:14877000-14880400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr7:14877000-14880400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr7:14877000-14881000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr7:14877000-14883200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr7:14877000-14886000 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr7:14877200-14880200 Weak transcription NH-A brain
10 chr7:14878000-14880600 Enhancers Placenta Amnion Placenta Amnion
11 chr7:14878200-14882600 Enhancers Osteobl bone
12 chr7:14879600-14882400 Enhancers NHDF-Ad bronchial
13 chr7:14879800-14880000 Flanking Active TSS Muscle Satellite Cultured Cells --
14 chr7:14879800-14882600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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