Variant report

Variant rs7141296
Chromosome Location chr14:104834961-104834962
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr14:104833600-104835000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr14:104833800-104835600 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr14:104834200-104836000 Bivalent Enhancer Fetal Stomach stomach
7 chr14:104834200-104836400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr14:104834400-104835000 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr14:104834600-104836400 Enhancers Brain Germinal Matrix brain
10 chr14:104834600-104838600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr14:104834800-104835000 Enhancers Fetal Lung lung
12 chr14:104834800-104835400 Enhancers Fetal Brain Male brain

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