Variant report

Variant rs181498770
Chromosome Location chr4:9862760-9862761
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 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 chr4:9858000-9862800 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
5 chr4:9858400-9867000 Strong transcription Monocytes-CD14+_RO01746 blood
6 chr4:9858800-9863200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr4:9861000-9864800 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr4:9861200-9863400 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:9861200-9863600 Strong transcription Liver Liver
10 chr4:9861400-9864400 Strong transcription Primary monocytes fromperipheralblood blood
11 chr4:9861600-9863800 Weak transcription Right Ventricle heart
12 chr4:9861600-9864400 Strong transcription HepG2 liver
13 chr4:9861600-9874400 Weak transcription Stomach Smooth Muscle stomach
14 chr4:9861800-9862800 Strong transcription Duodenum Mucosa Duodenum
15 chr4:9861800-9862800 Strong transcription Fetal Intestine Large intestine
16 chr4:9861800-9864200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr4:9862600-9863000 Weak transcription Adipose Nuclei Adipose
18 chr4:9862600-9863600 Weak transcription Duodenum Smooth Muscle Duodenum
19 chr4:9862600-9868200 Weak transcription Lung lung
20 chr4:9862600-9871600 Weak transcription Fetal Intestine Small intestine
21 chr4:9862600-9880400 Weak transcription HMEC breast
22 chr4:9862600-9883000 Weak transcription Esophagus oesophagus

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