Variant report

Variant rs551569160
Chromosome Location chr4:9864397-9864398
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9845000-9874800 Weak transcription NHEK skin
2 chr4:9851200-9869800 Weak transcription Gastric stomach
3 chr4:9857200-9864800 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr4:9858400-9867000 Strong transcription Monocytes-CD14+_RO01746 blood
5 chr4:9861000-9864800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
6 chr4:9861400-9864400 Strong transcription Primary monocytes fromperipheralblood blood
7 chr4:9861600-9864400 Strong transcription HepG2 liver
8 chr4:9861600-9874400 Weak transcription Stomach Smooth Muscle stomach
9 chr4:9862600-9868200 Weak transcription Lung lung
10 chr4:9862600-9871600 Weak transcription Fetal Intestine Small intestine
11 chr4:9862600-9880400 Weak transcription HMEC breast
12 chr4:9862600-9883000 Weak transcription Esophagus oesophagus
13 chr4:9862800-9871800 Strong transcription Breast Myoepithelial Primary Cells Breast
14 chr4:9862800-9880000 Weak transcription Fetal Intestine Large intestine
15 chr4:9862800-9887400 Weak transcription Duodenum Mucosa Duodenum
16 chr4:9863200-9868400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr4:9863400-9868200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr4:9863600-9887600 Weak transcription Liver Liver
19 chr4:9864200-9864400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell

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