Variant report

Variant rs59451543
Chromosome Location chr2:168508735-168508736
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:168504000-168509000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr2:168507400-168510400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr2:168507800-168509400 Enhancers HepG2 liver
4 chr2:168508000-168508800 Enhancers iPS-18 Cell Line embryonic stem cell
5 chr2:168508000-168509000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr2:168508000-168509000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:168508200-168508800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr2:168508200-168509400 Enhancers Cortex derived primary cultured neurospheres brain
9 chr2:168508400-168509000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr2:168508400-168519600 Weak transcription HUES48 Cell Line embryonic stem cell
11 chr2:168508400-168527200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr2:168508600-168508800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr2:168508600-168509000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr2:168508600-168509000 Enhancers NH-A brain
15 chr2:168508600-168520400 Weak transcription Fetal Brain Male brain

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