Variant report

Variant rs34874617
Chromosome Location chr11:121228918-121228919
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121224000-121230800 Weak transcription Right Atrium heart
2 chr11:121224200-121236000 Weak transcription Fetal Brain Female brain
3 chr11:121224600-121229600 Weak transcription Fetal Brain Male brain
4 chr11:121227800-121229600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:121228200-121229400 Enhancers Esophagus oesophagus
6 chr11:121228200-121229400 Enhancers Pancreas Pancrea
7 chr11:121228400-121229600 Enhancers Stomach Mucosa stomach
8 chr11:121228400-121229600 Enhancers HMEC breast
9 chr11:121228400-121230400 Enhancers Primary monocytes fromperipheralblood blood
10 chr11:121228400-121230800 Enhancers Breast Myoepithelial Primary Cells Breast
11 chr11:121228800-121229800 Weak transcription Primary hematopoietic stem cells blood
12 chr11:121228800-121230200 Flanking Active TSS Primary neutrophils fromperipheralblood blood

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