Variant report

Variant rs188260
Chromosome Location chr2:31553044-31553045
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:31528200-31554000 Weak transcription Right Ventricle heart
2 chr2:31547800-31556200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr2:31548000-31556000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr2:31548000-31556000 Weak transcription Skeletal Muscle Male skeletal muscle
5 chr2:31548000-31556200 Weak transcription Liver Liver
6 chr2:31548000-31556400 Weak transcription HMEC breast
7 chr2:31548000-31557600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:31548000-31558400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:31548000-31634600 Weak transcription Pancreatic Islets Pancreatic Islet
10 chr2:31548200-31553600 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr2:31548400-31558600 Weak transcription NHEK skin
12 chr2:31550600-31553600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr2:31552000-31553400 Enhancers Duodenum Mucosa Duodenum
14 chr2:31552200-31554000 Weak transcription Fetal Heart heart
15 chr2:31552400-31553400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr2:31552400-31556000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr2:31552800-31557000 Weak transcription Fetal Intestine Large intestine
18 chr2:31553000-31554000 Weak transcription Fetal Intestine Small intestine

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