Variant report

Variant rs16889522
Chromosome Location chr4:9849277-9849278
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9844800-9850600 Weak transcription HepG2 liver
2 chr4:9844800-9851000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:9845000-9851600 Weak transcription Fetal Intestine Small intestine
4 chr4:9845000-9874800 Weak transcription NHEK skin
5 chr4:9848200-9850600 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr4:9848400-9849400 Weak transcription Primary monocytes fromperipheralblood blood
7 chr4:9848600-9853200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr4:9848600-9861800 Weak transcription HMEC breast
9 chr4:9848800-9850200 Weak transcription Fetal Kidney kidney
10 chr4:9849200-9849800 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr4:9849200-9852400 Strong transcription Monocytes-CD14+_RO01746 blood

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