Variant report

Variant rs916365
Chromosome Location chr1:172453953-172453954
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172444200-172456200 Weak transcription Monocytes-CD14+_RO01746 blood
2 chr1:172450200-172456200 Weak transcription Primary T cells from cord blood blood
3 chr1:172450800-172456400 Enhancers Placenta Amnion Placenta Amnion
4 chr1:172452000-172457400 Weak transcription Fetal Intestine Small intestine
5 chr1:172452600-172454200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr1:172452600-172456600 Weak transcription Fetal Intestine Large intestine
7 chr1:172452800-172454000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:172452800-172454000 Enhancers HMEC breast
9 chr1:172453200-172454200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:172453200-172454200 Enhancers NHEK skin
11 chr1:172453200-172456200 Weak transcription Primary neutrophils fromperipheralblood blood
12 chr1:172453200-172456600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr1:172453600-172454200 Enhancers Primary monocytes fromperipheralblood blood
14 chr1:172453800-172454600 Enhancers Placenta Placenta
15 chr1:172453800-172455000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr1:172453800-172456400 Weak transcription Primary T helper 17 cells PMA-I stimulated --

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