Variant report

Variant rs10880755
Chromosome Location chr12:45572174-45572175
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:45565400-45586400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr12:45565600-45585000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:45567000-45572600 Weak transcription A549 lung
4 chr12:45568000-45572200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr12:45568200-45574200 ZNF genes & repeats hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
6 chr12:45569000-45574200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr12:45569400-45573400 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr12:45569600-45572800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr12:45570000-45593200 Weak transcription Placenta Amnion Placenta Amnion
10 chr12:45570200-45574000 ZNF genes & repeats Dnd41 blood
11 chr12:45570400-45572400 ZNF genes & repeats Duodenum Smooth Muscle Duodenum
12 chr12:45570600-45574000 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
13 chr12:45570800-45574200 ZNF genes & repeats Primary T cells from cord blood blood
14 chr12:45571000-45594600 Weak transcription Pancreas Pancrea
15 chr12:45571200-45572200 ZNF genes & repeats Primary T helper naive cells fromperipheralblood blood
16 chr12:45571600-45586000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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