Variant report

Variant rs4697649
Chromosome Location chr4:10703215-10703216
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:10695400-10706000 Weak transcription Ovary ovary
2 chr4:10698200-10703400 Weak transcription Fetal Thymus thymus
3 chr4:10698200-10706000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr4:10700800-10706000 Weak transcription GM12878-XiMat blood
5 chr4:10701600-10703400 Enhancers Stomach Mucosa stomach
6 chr4:10701600-10706200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr4:10701800-10705200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr4:10702000-10708600 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr4:10702000-10709000 Enhancers Primary hematopoietic stem cells blood
10 chr4:10703000-10704000 Enhancers Thymus Thymus
11 chr4:10703000-10706000 Weak transcription Fetal Adrenal Gland Adrenal Gland
12 chr4:10703000-10707000 Enhancers HSMM muscle
13 chr4:10703200-10704600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr4:10703200-10705400 Enhancers NH-A brain
15 chr4:10703200-10708200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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