Variant report

Variant rs16889932
Chromosome Location chr4:9877640-9877641
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9862600-9880400 Weak transcription HMEC breast
2 chr4:9862600-9883000 Weak transcription Esophagus oesophagus
3 chr4:9862800-9880000 Weak transcription Fetal Intestine Large intestine
4 chr4:9862800-9887400 Weak transcription Duodenum Mucosa Duodenum
5 chr4:9863600-9887600 Weak transcription Liver Liver
6 chr4:9870000-9878000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr4:9871000-9880800 Weak transcription Ovary ovary
8 chr4:9875800-9880800 Weak transcription NHEK skin
9 chr4:9876200-9879200 Weak transcription HepG2 liver
10 chr4:9876200-9879400 Weak transcription Fetal Intestine Small intestine
11 chr4:9876400-9879800 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr4:9876400-9880000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr4:9876400-9881000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr4:9877000-9878000 Enhancers Monocytes-CD14+_RO01746 blood
15 chr4:9877000-9878200 Enhancers Primary monocytes fromperipheralblood blood
16 chr4:9877400-9879200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr4:9877600-9877800 Weak transcription Aorta Aorta
18 chr4:9877600-9877800 Enhancers Fetal Heart heart

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