Variant report

Variant rs192703365
Chromosome Location chr4:9874692-9874693
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9845000-9874800 Weak transcription NHEK skin
2 chr4:9862600-9880400 Weak transcription HMEC breast
3 chr4:9862600-9883000 Weak transcription Esophagus oesophagus
4 chr4:9862800-9880000 Weak transcription Fetal Intestine Large intestine
5 chr4:9862800-9887400 Weak transcription Duodenum Mucosa Duodenum
6 chr4:9863600-9887600 Weak transcription Liver Liver
7 chr4:9864800-9877000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr4:9865800-9876200 Strong transcription HepG2 liver
9 chr4:9867000-9876400 Strong transcription Primary monocytes fromperipheralblood blood
10 chr4:9867800-9876400 Strong transcription Monocytes-CD14+_RO01746 blood
11 chr4:9869800-9874800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr4:9870000-9878000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr4:9871000-9880800 Weak transcription Ovary ovary
14 chr4:9872000-9876000 Weak transcription Aorta Aorta
15 chr4:9872200-9876400 Strong transcription Breast Myoepithelial Primary Cells Breast
16 chr4:9872400-9875000 Weak transcription Fetal Intestine Small intestine
17 chr4:9873200-9875000 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr4:9873600-9874800 Enhancers Fetal Brain Male brain

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