Variant report

Variant rs17097022
Chromosome Location chr12:46971036-46971037
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:46963000-46971200 Weak transcription Primary B cells from cord blood blood
2 chr12:46964000-46979400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr12:46965200-46975200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
4 chr12:46965200-46977600 Weak transcription Primary hematopoietic stem cells blood
5 chr12:46965800-46972200 Weak transcription NHDF-Ad bronchial
6 chr12:46967600-46972600 Weak transcription Primary B cells from peripheral blood blood
7 chr12:46967800-46972000 Weak transcription HSMMtube muscle
8 chr12:46967800-46972400 Weak transcription Psoas Muscle Psoas
9 chr12:46967800-46972400 Weak transcription Skeletal Muscle Male skeletal muscle
10 chr12:46968000-46972400 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr12:46969400-46972000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr12:46970000-46974600 Enhancers HepG2 liver
13 chr12:46970400-46971600 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr12:46970600-46971200 Enhancers NHEK skin
15 chr12:46970800-46971600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr12:46970800-46971600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr12:46970800-46971600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr12:46970800-46972200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr12:46970800-46972200 Enhancers HMEC breast
20 chr12:46971000-46971200 Enhancers iPS-15b Cell Line embryonic stem cell
21 chr12:46971000-46971200 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
22 chr12:46971000-46972200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
23 chr12:46971000-46973600 Enhancers Aorta Aorta

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