Variant report

Variant rs57994441
Chromosome Location chr6:167830329-167830330
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167829600-167830400 Bivalent Enhancer HepG2 liver
2 chr6:167829600-167833800 Weak transcription H1 Cell Line embryonic stem cell
3 chr6:167829600-167834800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:167829600-167841400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr6:167829800-167842200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr6:167830000-167830400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr6:167830000-167830600 Enhancers HUES6 Cell Line embryonic stem cell
8 chr6:167830200-167830400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr6:167830200-167830400 Flanking Active TSS Fetal Brain Male brain
10 chr6:167830200-167830800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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