Variant report

Variant rs33998698
Chromosome Location chr9:101566105-101566106
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:101559600-101567600 Weak transcription Stomach Smooth Muscle stomach
2 chr9:101559600-101567800 Weak transcription Stomach Mucosa stomach
3 chr9:101559600-101569000 Weak transcription Pancreas Pancrea
4 chr9:101559600-101569600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:101562600-101569400 Weak transcription H9 Cell Line embryonic stem cell
6 chr9:101564400-101567600 Weak transcription Duodenum Mucosa Duodenum
7 chr9:101564600-101566400 Weak transcription Colon Smooth Muscle Colon
8 chr9:101564600-101567600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr9:101564600-101567800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr9:101564800-101567400 Weak transcription HMEC breast
11 chr9:101564800-101567600 Weak transcription NHEK skin
12 chr9:101565400-101567800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr9:101565400-101569000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
14 chr9:101565800-101567400 Enhancers Fetal Lung lung
15 chr9:101565800-101567600 Enhancers Rectal Mucosa Donor 31 rectum
16 chr9:101566000-101566200 Enhancers Fetal Stomach stomach
17 chr9:101566000-101567400 Weak transcription K562 blood
18 chr9:101566000-101567600 Weak transcription Esophagus oesophagus

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