Variant report

Variant rs187016811
Chromosome Location chr4:9952110-9952111
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9911400-9979800 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr4:9928000-9960000 Weak transcription Esophagus oesophagus
3 chr4:9930800-9952200 Strong transcription Primary monocytes fromperipheralblood blood
4 chr4:9930800-9953800 Strong transcription Monocytes-CD14+_RO01746 blood
5 chr4:9938200-9957600 Weak transcription Fetal Stomach stomach
6 chr4:9939600-9956600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr4:9941400-9953200 Weak transcription Stomach Smooth Muscle stomach
8 chr4:9944000-9979400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
9 chr4:9944600-9964400 Weak transcription HMEC breast
10 chr4:9947600-9955800 Weak transcription Fetal Intestine Large intestine
11 chr4:9949000-9958400 Weak transcription NHEK skin
12 chr4:9949800-9979400 Weak transcription Liver Liver
13 chr4:9950000-9955000 Weak transcription Duodenum Mucosa Duodenum
14 chr4:9950000-9966600 Weak transcription Psoas Muscle Psoas
15 chr4:9950400-9954800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr4:9950400-9955800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr4:9950400-9959000 Weak transcription Right Atrium heart
18 chr4:9951200-9953800 Weak transcription Breast Myoepithelial Primary Cells Breast
19 chr4:9951800-9953000 Weak transcription HepG2 liver
20 chr4:9951800-9954800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
21 chr4:9951800-9955600 Weak transcription Fetal Intestine Small intestine

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