Variant report

Variant rs549878911
Chromosome Location chr4:9827589-9827590
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:9808200-9832000 Weak transcription Duodenum Mucosa Duodenum
2 chr4:9808800-9834400 Weak transcription NHEK skin
3 chr4:9810000-9830600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr4:9820200-9842600 Weak transcription HMEC breast
5 chr4:9820400-9833400 Weak transcription Esophagus oesophagus
6 chr4:9821000-9832400 Weak transcription Liver Liver
7 chr4:9821600-9833200 Weak transcription Fetal Intestine Small intestine
8 chr4:9822400-9828400 Strong transcription Monocytes-CD14+_RO01746 blood
9 chr4:9823800-9836400 Weak transcription Left Ventricle heart
10 chr4:9824000-9832400 Weak transcription Fetal Intestine Large intestine
11 chr4:9824400-9828400 Strong transcription Primary monocytes fromperipheralblood blood
12 chr4:9825800-9835000 Weak transcription Aorta Aorta
13 chr4:9826400-9827600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr4:9826400-9827600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr4:9826400-9827600 Enhancers Fetal Thymus thymus
16 chr4:9826400-9837600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr4:9826600-9828600 Strong transcription HepG2 liver
18 chr4:9827000-9827600 Enhancers Primary hematopoietic stem cells blood
19 chr4:9827000-9832400 Strong transcription Breast Myoepithelial Primary Cells Breast
20 chr4:9827400-9827600 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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