Variant report

Variant rs1056284
Chromosome Location chr11:10578767-10578768
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10573000-10603200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:10575000-10580200 Weak transcription Aorta Aorta
3 chr11:10576000-10585800 Weak transcription Placenta Placenta
4 chr11:10576200-10583600 Weak transcription Spleen Spleen
5 chr11:10578000-10578800 Enhancers H1 Cell Line embryonic stem cell
6 chr11:10578200-10578800 Enhancers Stomach Mucosa stomach
7 chr11:10578200-10583800 Weak transcription Primary B cells from peripheral blood blood
8 chr11:10578200-10590000 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr11:10578400-10579400 Enhancers Fetal Intestine Large intestine
10 chr11:10578400-10580000 Strong transcription Fetal Adrenal Gland Adrenal Gland
11 chr11:10578600-10578800 Enhancers Small Intestine intestine
12 chr11:10578600-10580600 Enhancers Fetal Intestine Small intestine
13 chr11:10578600-10585400 Weak transcription Fetal Stomach stomach

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