Variant report

Variant rs74089811
Chromosome Location chr14:105592668-105592669
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:105588000-105592800 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr14:105590400-105602600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr14:105590800-105593000 Enhancers Fetal Intestine Large intestine
4 chr14:105592200-105593400 Enhancers Duodenum Mucosa Duodenum
5 chr14:105592400-105593200 Enhancers Esophagus oesophagus
6 chr14:105592600-105593600 Enhancers Fetal Intestine Small intestine
7 chr14:105592600-105593800 Bivalent Enhancer HepG2 liver

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