Variant report

Variant rs12112157
Chromosome Location chr7:17695752-17695753
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17683800-17701800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr7:17691400-17696000 Enhancers NHDF-Ad bronchial
3 chr7:17692000-17701800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr7:17692600-17698800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr7:17693200-17699600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr7:17693400-17699000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr7:17693600-17695800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr7:17694000-17696000 Enhancers NHEK skin
9 chr7:17694600-17695800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr7:17695000-17700000 Weak transcription Osteobl bone
11 chr7:17695200-17699600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr7:17695200-17699800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr7:17695400-17700000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr7:17695600-17699800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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