Variant report

Variant rs9927599
Chromosome Location chr16:79665806-79665807
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:79662600-79666000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr16:79663000-79666000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr16:79663000-79666200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr16:79663200-79666000 Weak transcription Primary T cells fromperipheralblood blood
5 chr16:79663200-79666000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
6 chr16:79663200-79666200 Weak transcription Primary Natural Killer cells fromperipheralblood blood
7 chr16:79663400-79666000 Weak transcription HMEC breast
8 chr16:79664600-79667000 Weak transcription Fetal Intestine Small intestine
9 chr16:79665000-79666000 Enhancers Fetal Adrenal Gland Adrenal Gland
10 chr16:79665800-79666400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr16:79665800-79666800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr16:79665800-79666800 Enhancers Primary T helper memory cells from peripheral blood 1 blood
13 chr16:79665800-79666800 Enhancers Primary T helper 17 cells PMA-I stimulated --
14 chr16:79665800-79666800 Enhancers NHEK skin
15 chr16:79665800-79667000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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