Variant report

Variant rs4147872
Chromosome Location chr1:94461538-94461539
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:94446200-94463400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:94452400-94463800 Enhancers HMEC breast
3 chr1:94452800-94462400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:94452800-94464000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr1:94458200-94462000 Enhancers NHEK skin
6 chr1:94458600-94461800 Enhancers HSMM muscle
7 chr1:94458800-94477000 Weak transcription Right Atrium heart
8 chr1:94459000-94461800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:94459600-94463400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr1:94460400-94462000 Enhancers NH-A brain
11 chr1:94461000-94461600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:94461200-94461600 Flanking Active TSS HSMMtube muscle
13 chr1:94461400-94461800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr1:94461400-94462000 Enhancers Primary Natural Killer cells fromperipheralblood blood
15 chr1:94461400-94462000 Enhancers Pancreas Pancrea
16 chr1:94461400-94462200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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