Variant report

Variant rs11852081
Chromosome Location chr14:44369021-44369022
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:44365600-44369400 Weak transcription Fetal Intestine Small intestine
2 chr14:44368000-44369400 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr14:44368200-44369400 Weak transcription ES-WA7 Cell Line embryonic stem cell
4 chr14:44368200-44369400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr14:44369000-44370200 Flanking Active TSS HepG2 liver
6 chr14:44369000-44371200 Enhancers Fetal Intestine Large intestine

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