Variant report

Variant rs67941359
Chromosome Location chr14:104835757-104835758
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104831000-104842000 Weak transcription Gastric stomach
2 chr14:104831400-104838800 Weak transcription Fetal Intestine Small intestine
3 chr14:104833400-104837600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr14:104834200-104836000 Bivalent Enhancer Fetal Stomach stomach
5 chr14:104834200-104836400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr14:104834600-104836400 Enhancers Brain Germinal Matrix brain
7 chr14:104834600-104838600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr14:104835000-104835800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr14:104835000-104836000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr14:104835400-104842000 Weak transcription Fetal Brain Male brain
11 chr14:104835600-104836000 Enhancers ES-WA7 Cell Line embryonic stem cell

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