Variant report

Variant rs11038404
Chromosome Location chr11:45360514-45360515
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:45355200-45361000 Weak transcription Fetal Kidney kidney
2 chr11:45355600-45361200 Weak transcription Fetal Stomach stomach
3 chr11:45356200-45360600 Weak transcription Fetal Brain Male brain
4 chr11:45356400-45361000 Weak transcription Fetal Brain Female brain
5 chr11:45357400-45361400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr11:45358400-45361200 Weak transcription Duodenum Mucosa Duodenum
7 chr11:45359400-45362200 Enhancers Fetal Adrenal Gland Adrenal Gland
8 chr11:45359600-45360800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr11:45359800-45361400 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr11:45359800-45361600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr11:45359800-45361600 Weak transcription NHEK skin
12 chr11:45359800-45361800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr11:45360000-45361400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr11:45360000-45361800 Weak transcription HMEC breast
15 chr11:45360400-45360600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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