Variant report

Variant rs542108158
Chromosome Location chr2:50877951-50877952
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50874800-50878000 Enhancers HUES48 Cell Line embryonic stem cell
2 chr2:50875600-50878000 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr2:50875800-50878000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr2:50876000-50878800 Weak transcription Brain Hippocampus Middle brain
5 chr2:50876000-50878800 Weak transcription Brain Substantia Nigra brain
6 chr2:50876000-50878800 Weak transcription Fetal Brain Female brain
7 chr2:50876200-50879200 Weak transcription Brain Cingulate Gyrus brain
8 chr2:50876400-50878200 Enhancers HUES64 Cell Line embryonic stem cell
9 chr2:50876400-50879800 Enhancers HMEC breast
10 chr2:50876800-50878000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr2:50876800-50878000 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr2:50877000-50878000 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr2:50877000-50878000 Flanking Active TSS NHEK skin
14 chr2:50877000-50879200 Enhancers Brain Germinal Matrix brain
15 chr2:50877400-50879000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr2:50877600-50879000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr2:50877800-50878200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr2:50877800-50878800 Weak transcription Cortex derived primary cultured neurospheres brain

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