Variant report

Variant rs72945524
Chromosome Location chr11:77280090-77280091
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:77272400-77282600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr11:77278400-77280800 Enhancers Fetal Intestine Large intestine
3 chr11:77278400-77282600 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr11:77278400-77283000 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr11:77278600-77280200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr11:77279000-77280800 Enhancers Fetal Intestine Small intestine
7 chr11:77279000-77281600 Enhancers Ovary ovary
8 chr11:77279200-77281000 Enhancers Duodenum Mucosa Duodenum
9 chr11:77279200-77283800 Enhancers Pancreas Pancrea
10 chr11:77279400-77281600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr11:77279600-77284800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr11:77279800-77280600 Enhancers Placenta Placenta
13 chr11:77279800-77280800 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr11:77280000-77280400 Enhancers ES-WA7 Cell Line embryonic stem cell
15 chr11:77280000-77280600 Enhancers H9 Cell Line embryonic stem cell
16 chr11:77280000-77280600 Enhancers HUES6 Cell Line embryonic stem cell
17 chr11:77280000-77281000 Enhancers iPS-15b Cell Line embryonic stem cell
18 chr11:77280000-77282800 Enhancers Fetal Stomach stomach

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