Variant report

Variant rs12808728
Chromosome Location chr11:119723399-119723400
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:119716200-119723400 Weak transcription Fetal Intestine Large intestine
2 chr11:119716200-119725200 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr11:119716400-119724400 Weak transcription Right Atrium heart
4 chr11:119717200-119723600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:119717800-119723400 Weak transcription Fetal Intestine Small intestine
6 chr11:119719000-119724400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr11:119722200-119723600 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr11:119722200-119724800 Weak transcription Brain Substantia Nigra brain
9 chr11:119722200-119729600 Weak transcription H9 Cell Line embryonic stem cell
10 chr11:119722800-119725000 Weak transcription Right Ventricle heart
11 chr11:119723000-119724800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr11:119723200-119723400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
13 chr11:119723200-119723800 Enhancers Duodenum Mucosa Duodenum

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