Variant report

Variant rs10850849
Chromosome Location chr12:118032637-118032638
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:118021800-118036800 Weak transcription H9 Cell Line embryonic stem cell
2 chr12:118030800-118032800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr12:118030800-118033000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr12:118031000-118032800 Enhancers Fetal Intestine Large intestine
5 chr12:118031200-118032800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr12:118031400-118032800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr12:118031400-118036800 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr12:118031600-118041000 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr12:118031600-118041400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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