Variant report

Variant rs6929962
Chromosome Location chr6:44708031-44708032
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:44703800-44708400 Weak transcription Placenta Placenta
2 chr6:44705200-44709400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr6:44705400-44709000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr6:44705600-44708400 Enhancers Adipose Nuclei Adipose
5 chr6:44705800-44709000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr6:44706600-44710400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr6:44706800-44708600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr6:44706800-44710400 Weak transcription Duodenum Mucosa Duodenum
9 chr6:44707200-44708400 Weak transcription Fetal Brain Male brain
10 chr6:44707600-44710000 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr6:44707800-44709000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr6:44707800-44710000 Weak transcription Fetal Intestine Small intestine
13 chr6:44708000-44709600 Weak transcription ES-WA7 Cell Line embryonic stem cell
14 chr6:44708000-44710000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
15 chr6:44708000-44710000 Weak transcription Fetal Intestine Large intestine

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