Variant report

Variant rs12084940
Chromosome Location chr1:77512145-77512146
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77497000-77516800 Weak transcription Fetal Stomach stomach
2 chr1:77503800-77512200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr1:77506000-77558600 Weak transcription Stomach Smooth Muscle stomach
4 chr1:77508600-77547600 Weak transcription Ovary ovary
5 chr1:77509600-77515200 Strong transcription Cortex derived primary cultured neurospheres brain
6 chr1:77510400-77515800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr1:77510400-77517000 Weak transcription Aorta Aorta
8 chr1:77510600-77517000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:77510600-77517200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:77510800-77515800 Weak transcription NHEK skin
11 chr1:77511000-77516000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
12 chr1:77511200-77517000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:77511600-77513600 Weak transcription Monocytes-CD14+_RO01746 blood
14 chr1:77511800-77520600 Weak transcription Brain Angular Gyrus brain
15 chr1:77512000-77512400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
16 chr1:77512000-77513600 Weak transcription Primary monocytes fromperipheralblood blood

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