Variant report

Variant rs74088570
Chromosome Location chr14:104830595-104830596
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104825000-104830600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr14:104827400-104831000 Enhancers Fetal Intestine Small intestine
3 chr14:104828400-104831000 Enhancers Gastric stomach
4 chr14:104829200-104831000 Enhancers Fetal Intestine Large intestine
5 chr14:104829800-104830800 Enhancers Stomach Mucosa stomach
6 chr14:104830000-104831000 Enhancers Pancreas Pancrea
7 chr14:104830400-104830800 Bivalent Enhancer Fetal Muscle Trunk muscle

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