Variant report

Variant rs563822249
Chromosome Location chr2:50878625-50878626
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50876000-50878800 Weak transcription Brain Hippocampus Middle brain
2 chr2:50876000-50878800 Weak transcription Brain Substantia Nigra brain
3 chr2:50876000-50878800 Weak transcription Fetal Brain Female brain
4 chr2:50876200-50879200 Weak transcription Brain Cingulate Gyrus brain
5 chr2:50876400-50879800 Enhancers HMEC breast
6 chr2:50877000-50879200 Enhancers Brain Germinal Matrix brain
7 chr2:50877400-50879000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr2:50877600-50879000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:50877800-50878800 Weak transcription Cortex derived primary cultured neurospheres brain
10 chr2:50878000-50879000 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr2:50878000-50879400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr2:50878000-50879800 Enhancers NHEK skin
13 chr2:50878200-50878800 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr2:50878200-50880000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr2:50878600-50879200 Enhancers Brain Dorsolateral Prefrontal Cortex brain

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