Variant report

Variant rs16843627
Chromosome Location chr3:100997814-100997815
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:100958800-101012800 Weak transcription Left Ventricle heart
2 chr3:100980800-100998000 Weak transcription HSMM muscle
3 chr3:100982400-100998800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr3:100986600-100998400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr3:100988400-100998000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr3:100989400-101018600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr3:100991800-100998200 Weak transcription HSMMtube muscle
8 chr3:100994800-101008800 Weak transcription Primary T cells from cord blood blood
9 chr3:100997400-101000600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr3:100997800-100998200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr3:100997800-100998400 Enhancers NHDF-Ad bronchial
12 chr3:100997800-100998800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr3:100997800-100999200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr3:100997800-100999200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr3:100997800-100999200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr3:100997800-100999400 Enhancers HMEC breast

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