Variant report

Variant rs10845221
Chromosome Location chr12:10989534-10989535
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:10973600-11009600 Weak transcription HSMM muscle
2 chr12:10987400-10989600 Weak transcription Aorta Aorta
3 chr12:10988000-10995400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr12:10988400-11006000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr12:10988400-11008400 Weak transcription Rectal Mucosa Donor 29 rectum
6 chr12:10988600-10995600 Weak transcription Stomach Smooth Muscle stomach
7 chr12:10988800-11001600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr12:10989200-10989600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr12:10989200-10990200 ZNF genes & repeats Fetal Muscle Leg muscle
10 chr12:10989200-10999200 Weak transcription Fetal Adrenal Gland Adrenal Gland
11 chr12:10989200-11008600 Weak transcription Brain Cingulate Gyrus brain
12 chr12:10989400-10989600 ZNF genes & repeats Primary T cells from cord blood blood
13 chr12:10989400-10990200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr12:10989400-10995800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
15 chr12:10989400-11008200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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