Variant report

Variant rs72896525
Chromosome Location chr4:110911539-110911540
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:110895000-110928600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr4:110901000-110929600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:110901400-110920800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr4:110906800-110920800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr4:110907000-110932400 Weak transcription Psoas Muscle Psoas
6 chr4:110907800-110927400 Weak transcription Skeletal Muscle Male skeletal muscle
7 chr4:110908600-110916200 Strong transcription Skeletal Muscle Female skeletal muscle
8 chr4:110909600-110912000 Enhancers HMEC breast
9 chr4:110909600-110913800 Enhancers Primary monocytes fromperipheralblood blood
10 chr4:110909800-110911600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr4:110910200-110911600 Weak transcription Esophagus oesophagus
12 chr4:110910200-110920400 Weak transcription Fetal Intestine Small intestine
13 chr4:110910400-110935200 Weak transcription Pancreas Pancrea
14 chr4:110910600-110929800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr4:110910800-110926800 Weak transcription Fetal Heart heart
16 chr4:110911000-110911800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr4:110911000-110912000 Enhancers NHEK skin
18 chr4:110911200-110912200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr4:110911200-110912800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
20 chr4:110911200-110913400 ZNF genes & repeats Primary B cells from peripheral blood blood
21 chr4:110911400-110912200 Flanking Active TSS GM12878-XiMat blood

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