Variant report

Variant rs9425628
Chromosome Location chr1:172451442-172451443
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172444200-172456200 Weak transcription Monocytes-CD14+_RO01746 blood
2 chr1:172445000-172452400 Weak transcription Primary neutrophils fromperipheralblood blood
3 chr1:172445800-172451600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:172447600-172452800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr1:172448200-172452600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:172448200-172452800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:172448400-172452800 Weak transcription HMEC breast
8 chr1:172448600-172453200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:172448600-172453200 Weak transcription NHEK skin
10 chr1:172449800-172451600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr1:172449800-172453000 Weak transcription Placenta Placenta
12 chr1:172450000-172452800 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr1:172450200-172456200 Weak transcription Primary T cells from cord blood blood
14 chr1:172450800-172451600 Enhancers HepG2 liver
15 chr1:172450800-172452600 Enhancers Fetal Intestine Large intestine
16 chr1:172450800-172456400 Enhancers Placenta Amnion Placenta Amnion
17 chr1:172451000-172451600 Enhancers A549 lung
18 chr1:172451000-172452000 Enhancers Fetal Intestine Small intestine

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