Variant report

Variant rs11933838
Chromosome Location chr4:9852920-9852921
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9845000-9874800 Weak transcription NHEK skin
2 chr4:9848600-9853200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr4:9848600-9861800 Weak transcription HMEC breast
4 chr4:9850200-9858800 Weak transcription Primary monocytes fromperipheralblood blood
5 chr4:9850600-9853000 Strong transcription Breast Myoepithelial Primary Cells Breast
6 chr4:9851200-9869800 Weak transcription Gastric stomach
7 chr4:9851400-9859000 Weak transcription HepG2 liver
8 chr4:9851600-9857200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr4:9852200-9858200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr4:9852400-9858400 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr4:9852400-9858800 Weak transcription Fetal Intestine Small intestine
12 chr4:9852600-9853000 Enhancers H1 Cell Line embryonic stem cell
13 chr4:9852800-9853200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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