Variant report

Variant rs150612332
Chromosome Location chr10:5122096-5122097
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:5119000-5122600 Weak transcription Adipose Nuclei Adipose
2 chr10:5119800-5124000 Weak transcription NHDF-Ad bronchial
3 chr10:5119800-5124400 Weak transcription Muscle Satellite Cultured Cells --
4 chr10:5120400-5124800 Enhancers Stomach Mucosa stomach
5 chr10:5120600-5122600 Flanking Active TSS A549 lung
6 chr10:5120600-5124600 Enhancers HepG2 liver
7 chr10:5120800-5123600 Enhancers Fetal Intestine Small intestine
8 chr10:5121000-5122200 Enhancers HUES64 Cell Line embryonic stem cell
9 chr10:5121000-5122400 Enhancers Duodenum Mucosa Duodenum
10 chr10:5121000-5123400 Enhancers Fetal Intestine Large intestine
11 chr10:5121200-5122200 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr10:5121200-5122400 Enhancers Small Intestine intestine
13 chr10:5121600-5122200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr10:5121600-5123000 Enhancers K562 blood
15 chr10:5121800-5124000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr10:5122000-5132200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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