Variant report

Variant rs456818
Chromosome Location chr21:41160242-41160243
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:41149400-41160400 Weak transcription Placenta Placenta
2 chr21:41156800-41160800 Weak transcription Placenta Amnion Placenta Amnion
3 chr21:41160000-41163600 Enhancers Fetal Heart heart
4 chr21:41160200-41160400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr21:41160200-41160400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr21:41160200-41160400 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr21:41160200-41160400 Enhancers Brain Substantia Nigra brain
8 chr21:41160200-41160400 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr21:41160200-41160400 Enhancers Fetal Kidney kidney
10 chr21:41160200-41160400 Enhancers Stomach Mucosa stomach
11 chr21:41160200-41160600 Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr21:41160200-41160600 Enhancers Brain Inferior Temporal Lobe brain
13 chr21:41160200-41160600 Active TSS Brain Dorsolateral Prefrontal Cortex brain
14 chr21:41160200-41160600 Enhancers Colon Smooth Muscle Colon
15 chr21:41160200-41160800 Enhancers Rectal Smooth Muscle rectum
16 chr21:41160200-41160800 Enhancers Stomach Smooth Muscle stomach
17 chr21:41160200-41161400 Enhancers Breast Myoepithelial Primary Cells Breast

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