Variant report

Variant rs201179899
Chromosome Location chr4:26491923-26491924
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:26490600-26492000 Active TSS Gastric stomach
2 chr4:26490600-26492400 Bivalent Enhancer Fetal Brain Male brain
3 chr4:26490800-26492000 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr4:26490800-26492200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr4:26490800-26492600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr4:26491000-26492600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr4:26491200-26493000 Enhancers Fetal Lung lung
8 chr4:26491400-26492200 Bivalent Enhancer Brain Germinal Matrix brain
9 chr4:26491400-26492400 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
10 chr4:26491400-26492600 Flanking Active TSS Cortex derived primary cultured neurospheres brain
11 chr4:26491400-26494600 Weak transcription Right Atrium heart
12 chr4:26491800-26492000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr4:26491800-26492200 Active TSS Fetal Brain Female brain
14 chr4:26491800-26492200 Flanking Bivalent TSS/Enh Fetal Stomach stomach

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