Variant report

Variant rs55996632
Chromosome Location chr17:43935888-43935889
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43929200-43942000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr17:43935200-43936000 Enhancers Brain Cingulate Gyrus brain
3 chr17:43935200-43936000 Enhancers Brain Dorsolateral Prefrontal Cortex brain
4 chr17:43935200-43936200 Enhancers Brain Anterior Caudate brain
5 chr17:43935200-43936200 Enhancers Brain Inferior Temporal Lobe brain
6 chr17:43935400-43936000 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr17:43935400-43936000 Enhancers Right Atrium heart
8 chr17:43935400-43936200 Enhancers Adipose Nuclei Adipose
9 chr17:43935400-43936200 Enhancers Brain Hippocampus Middle brain
10 chr17:43935400-43936400 Enhancers Brain Substantia Nigra brain
11 chr17:43935600-43936000 Enhancers Brain Angular Gyrus brain
12 chr17:43935800-43936000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr17:43935800-43936000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
14 chr17:43935800-43936000 Bivalent Enhancer Skeletal Muscle Female skeletal muscle

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