Variant report

Variant rs35796129
Chromosome Location chr14:71758598-71758599
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:71755800-71758600 Enhancers Placenta Placenta
2 chr14:71756600-71763000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr14:71757600-71758600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr14:71757600-71758600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr14:71757600-71758600 Enhancers HUVEC blood vessel
6 chr14:71757600-71758800 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr14:71757800-71758600 Enhancers Ovary ovary
8 chr14:71757800-71758600 Enhancers NH-A brain
9 chr14:71757800-71758600 Enhancers NHEK skin
10 chr14:71758200-71758600 Enhancers GM12878-XiMat blood
11 chr14:71758400-71759400 Weak transcription Primary monocytes fromperipheralblood blood
12 chr14:71758400-71761600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr14:71758400-71767000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr14:71758400-71770000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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