Variant report

Variant rs13404615
Chromosome Location chr2:51178352-51178353
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:51176200-51181400 Weak transcription Brain Germinal Matrix brain
2 chr2:51176400-51190600 Weak transcription iPS-15b Cell Line embryonic stem cell
3 chr2:51177200-51181800 Weak transcription Brain Substantia Nigra brain
4 chr2:51177400-51179600 Weak transcription Pancreatic Islets Pancreatic Islet
5 chr2:51177400-51182400 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr2:51177800-51179800 Enhancers Hela-S3 cervix
7 chr2:51178000-51178600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:51178000-51180000 Enhancers HMEC breast
9 chr2:51178200-51178600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr2:51178200-51178600 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr2:51178200-51178600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr2:51178200-51178800 Enhancers HUES48 Cell Line embryonic stem cell
13 chr2:51178200-51179000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr2:51178200-51179600 Enhancers NHEK skin

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