Variant report

Variant rs566711547
Chromosome Location chr2:50879081-50879082
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50876200-50879200 Weak transcription Brain Cingulate Gyrus brain
2 chr2:50876400-50879800 Enhancers HMEC breast
3 chr2:50877000-50879200 Enhancers Brain Germinal Matrix brain
4 chr2:50878000-50879400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:50878000-50879800 Enhancers NHEK skin
6 chr2:50878200-50880000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:50878600-50879200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
8 chr2:50878800-50879400 Enhancers Brain Hippocampus Middle brain
9 chr2:50878800-50879400 Enhancers Fetal Brain Female brain
10 chr2:50878800-50879800 Enhancers Cortex derived primary cultured neurospheres brain
11 chr2:50879000-50879200 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr2:50879000-50879400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr2:50879000-50879400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr2:50879000-50879400 Weak transcription Brain Substantia Nigra brain
15 chr2:50879000-50879800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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