Variant report

Variant rs2382551
Chromosome Location chr9:16033443-16033444
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:16023600-16040600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr9:16026200-16039200 Weak transcription Adipose Nuclei Adipose
3 chr9:16026400-16039200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr9:16030400-16034400 Enhancers NHEK skin
5 chr9:16030800-16050000 Weak transcription Aorta Aorta
6 chr9:16031000-16033800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr9:16031200-16034400 Enhancers HSMM muscle
8 chr9:16031600-16034200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr9:16031600-16035600 Enhancers Fetal Muscle Leg muscle
10 chr9:16032200-16033800 Weak transcription Fetal Muscle Trunk muscle
11 chr9:16032200-16034000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr9:16032200-16035000 Weak transcription Dnd41 blood
13 chr9:16032200-16039200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr9:16032800-16037400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr9:16033000-16033800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr9:16033000-16035200 Weak transcription HMEC breast
17 chr9:16033200-16039200 Weak transcription Stomach Smooth Muscle stomach
18 chr9:16033400-16039200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
19 chr9:16033400-16039200 Weak transcription Osteobl bone

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