Variant report

Variant rs10495991
Chromosome Location chr2:50227864-50227865
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:50223400-50233000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr2:50226200-50229000 Weak transcription H1 Cell Line embryonic stem cell
3 chr2:50226200-50229000 Weak transcription HUES48 Cell Line embryonic stem cell
4 chr2:50227000-50228000 Enhancers Fetal Intestine Small intestine
5 chr2:50227200-50229200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr2:50227400-50232600 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr2:50227600-50229000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr2:50227800-50228000 Enhancers H9 Cell Line embryonic stem cell
9 chr2:50227800-50228400 Enhancers Fetal Intestine Large intestine

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