Variant report

Variant rs59635491
Chromosome Location chr2:21490274-21490275
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:21479000-21490400 Weak transcription Spleen Spleen
2 chr2:21479400-21494800 Enhancers Brain Substantia Nigra brain
3 chr2:21483400-21490600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:21485000-21490400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr2:21488800-21490400 Weak transcription K562 blood
6 chr2:21488800-21490800 Weak transcription Aorta Aorta
7 chr2:21489000-21492600 Enhancers Ovary ovary
8 chr2:21489600-21491000 Enhancers Brain Inferior Temporal Lobe brain
9 chr2:21489600-21495400 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr2:21489800-21492000 Enhancers Pancreas Pancrea
11 chr2:21489800-21492200 Enhancers Brain Hippocampus Middle brain
12 chr2:21489800-21492400 Enhancers Brain Angular Gyrus brain
13 chr2:21489800-21494200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
14 chr2:21489800-21494600 Enhancers Brain Anterior Caudate brain
15 chr2:21489800-21494600 Enhancers Brain Cingulate Gyrus brain
16 chr2:21489800-21495200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr2:21490200-21490600 Enhancers Fetal Lung lung
18 chr2:21490200-21490800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr2:21490200-21490800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
20 chr2:21490200-21491200 Bivalent Enhancer Fetal Stomach stomach
21 chr2:21490200-21494400 Enhancers Fetal Kidney kidney

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