Variant report

Variant rs1009803
Chromosome Location chr1:172452422-172452423
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172444200-172456200 Weak transcription Monocytes-CD14+_RO01746 blood
2 chr1:172447600-172452800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr1:172448200-172452600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:172448200-172452800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:172448400-172452800 Weak transcription HMEC breast
6 chr1:172448600-172453200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:172448600-172453200 Weak transcription NHEK skin
8 chr1:172449800-172453000 Weak transcription Placenta Placenta
9 chr1:172450000-172452800 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr1:172450200-172456200 Weak transcription Primary T cells from cord blood blood
11 chr1:172450800-172452600 Enhancers Fetal Intestine Large intestine
12 chr1:172450800-172456400 Enhancers Placenta Amnion Placenta Amnion
13 chr1:172451600-172452600 Weak transcription A549 lung
14 chr1:172451600-172453000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr1:172451600-172453000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr1:172452000-172457400 Weak transcription Fetal Intestine Small intestine
17 chr1:172452400-172453200 Enhancers Primary neutrophils fromperipheralblood blood

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