Variant report

Variant rs4143724
Chromosome Location chr15:51870413-51870414
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:51867800-51872400 Enhancers K562 blood
2 chr15:51868200-51870800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr15:51868600-51872000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
4 chr15:51868800-51870800 Enhancers Colon Smooth Muscle Colon
5 chr15:51869000-51871600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr15:51869600-51870800 Weak transcription Small Intestine intestine
7 chr15:51869600-51875200 Enhancers Primary neutrophils fromperipheralblood blood
8 chr15:51869600-51889600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr15:51869800-51870800 Enhancers Primary B cells from cord blood blood
10 chr15:51870000-51875200 Enhancers Primary monocytes fromperipheralblood blood
11 chr15:51870200-51871200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr15:51870200-51871200 Weak transcription Primary hematopoietic stem cells short term culture blood
13 chr15:51870200-51871200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr15:51870200-51871200 Weak transcription Adipose Nuclei Adipose
15 chr15:51870400-51871600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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