Variant report

Variant rs10402559
Chromosome Location chr19:43160350-43160351
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:43156000-43162000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chr19:43157800-43163000 Enhancers Adipose Nuclei Adipose
3 chr19:43158600-43162400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr19:43159200-43163000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr19:43159400-43162000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr19:43159800-43160600 Enhancers Pancreas Pancrea
7 chr19:43159800-43161800 Enhancers Brain Inferior Temporal Lobe brain
8 chr19:43159800-43161800 Enhancers Brain Substantia Nigra brain
9 chr19:43159800-43162000 Enhancers Brain Hippocampus Middle brain
10 chr19:43160000-43160400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
11 chr19:43160000-43160600 Enhancers Gastric stomach
12 chr19:43160000-43161400 Enhancers Brain Anterior Caudate brain
13 chr19:43160000-43161600 Enhancers Brain Cingulate Gyrus brain
14 chr19:43160000-43162000 Enhancers Brain Angular Gyrus brain
15 chr19:43160200-43161800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr19:43160200-43174800 Weak transcription Fetal Adrenal Gland Adrenal Gland

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