Variant report

Variant rs12498150
Chromosome Location chr4:9950537-9950538
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9911400-9979800 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr4:9926400-9951600 Weak transcription Spleen Spleen
3 chr4:9928000-9960000 Weak transcription Esophagus oesophagus
4 chr4:9930800-9952200 Strong transcription Primary monocytes fromperipheralblood blood
5 chr4:9930800-9953800 Strong transcription Monocytes-CD14+_RO01746 blood
6 chr4:9933600-9951200 Strong transcription Breast Myoepithelial Primary Cells Breast
7 chr4:9938200-9957600 Weak transcription Fetal Stomach stomach
8 chr4:9939600-9956600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr4:9941400-9953200 Weak transcription Stomach Smooth Muscle stomach
10 chr4:9944000-9979400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
11 chr4:9944600-9964400 Weak transcription HMEC breast
12 chr4:9947400-9951800 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr4:9947600-9955800 Weak transcription Fetal Intestine Large intestine
14 chr4:9948600-9950800 Genic enhancers HepG2 liver
15 chr4:9949000-9958400 Weak transcription NHEK skin
16 chr4:9949800-9979400 Weak transcription Liver Liver
17 chr4:9950000-9955000 Weak transcription Duodenum Mucosa Duodenum
18 chr4:9950000-9966600 Weak transcription Psoas Muscle Psoas
19 chr4:9950200-9951400 Weak transcription Left Ventricle heart
20 chr4:9950200-9951600 Weak transcription Right Ventricle heart
21 chr4:9950400-9951800 Strong transcription Fetal Intestine Small intestine
22 chr4:9950400-9952000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
23 chr4:9950400-9954800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
24 chr4:9950400-9955800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
25 chr4:9950400-9959000 Weak transcription Right Atrium heart

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