Variant report

Variant rs150352262
Chromosome Location chr4:9957294-9957295
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr4:9938200-9957600 Weak transcription Fetal Stomach stomach
4 chr4:9944000-9979400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
5 chr4:9944600-9964400 Weak transcription HMEC breast
6 chr4:9949000-9958400 Weak transcription NHEK skin
7 chr4:9949800-9979400 Weak transcription Liver Liver
8 chr4:9950000-9966600 Weak transcription Psoas Muscle Psoas
9 chr4:9950400-9959000 Weak transcription Right Atrium heart
10 chr4:9954800-9957400 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr4:9954800-9958800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr4:9955400-9964000 Weak transcription Duodenum Mucosa Duodenum
13 chr4:9955800-9959000 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr4:9956000-9960000 Strong transcription Primary monocytes fromperipheralblood blood
15 chr4:9956000-9962800 Strong transcription HepG2 liver
16 chr4:9956000-9963200 Strong transcription Monocytes-CD14+_RO01746 blood
17 chr4:9956600-9958400 Weak transcription Breast Myoepithelial Primary Cells Breast
18 chr4:9956600-9964200 Weak transcription Fetal Intestine Large intestine
19 chr4:9956800-9964000 Weak transcription Fetal Intestine Small intestine

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