Variant report

Variant rs183429116
Chromosome Location chr12:60592037-60592038
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:60586000-60603400 Weak transcription HMEC breast
2 chr12:60589200-60595400 Weak transcription NHDF-Ad bronchial
3 chr12:60589200-60595800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr12:60589200-60598200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr12:60589600-60593400 Weak transcription K562 blood
6 chr12:60590600-60592200 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr12:60591200-60592200 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr12:60591600-60592200 Enhancers A549 lung
9 chr12:60591600-60595800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr12:60591800-60592200 Enhancers HUES6 Cell Line embryonic stem cell
11 chr12:60591800-60593400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr12:60592000-60592200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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