Variant report

Variant rs10889038
Chromosome Location chr1:57826766-57826767
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57819400-57832000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr1:57823800-57833200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:57826000-57827000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr1:57826000-57827400 Enhancers Fetal Brain Female brain
5 chr1:57826000-57829600 Enhancers Fetal Heart heart
6 chr1:57826400-57827000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:57826400-57827600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
8 chr1:57826600-57826800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr1:57826600-57826800 Enhancers Left Ventricle heart
10 chr1:57826600-57827000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr1:57826600-57827400 Enhancers Fetal Brain Male brain
12 chr1:57826600-57827400 Enhancers Fetal Stomach stomach

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