Variant report

Variant rs537393052
Chromosome Location chr10:5120838-5120839
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:5113200-5121000 Weak transcription Gastric stomach
2 chr10:5114600-5121000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr10:5114600-5121400 Weak transcription Fetal Kidney kidney
4 chr10:5116200-5121000 Weak transcription Fetal Intestine Large intestine
5 chr10:5116200-5121200 Weak transcription Small Intestine intestine
6 chr10:5119000-5122600 Weak transcription Adipose Nuclei Adipose
7 chr10:5119800-5121600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr10:5119800-5124000 Weak transcription NHDF-Ad bronchial
9 chr10:5119800-5124400 Weak transcription Muscle Satellite Cultured Cells --
10 chr10:5120000-5121000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr10:5120400-5121000 Enhancers K562 blood
12 chr10:5120400-5124800 Enhancers Stomach Mucosa stomach
13 chr10:5120600-5121600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr10:5120600-5122000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr10:5120600-5122000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr10:5120600-5122600 Flanking Active TSS A549 lung
17 chr10:5120600-5124600 Enhancers HepG2 liver
18 chr10:5120800-5121600 Enhancers Hela-S3 cervix
19 chr10:5120800-5121800 Enhancers HMEC breast
20 chr10:5120800-5123600 Enhancers Fetal Intestine Small intestine

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