Variant report

Variant rs12344866
Chromosome Location chr9:599666-599667
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:590000-625000 Weak transcription Aorta Aorta
2 chr9:590200-600200 Weak transcription Placenta Placenta
3 chr9:590200-621600 Weak transcription Psoas Muscle Psoas
4 chr9:591400-601600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr9:592600-607200 Weak transcription Pancreas Pancrea
6 chr9:592600-614400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr9:592800-602600 Weak transcription NHEK skin
8 chr9:593000-602800 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr9:593000-602800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr9:593000-606800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr9:593000-608600 Weak transcription Esophagus oesophagus
12 chr9:593200-606800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr9:595600-614000 Weak transcription Right Ventricle heart
14 chr9:596600-605600 Weak transcription Brain Hippocampus Middle brain
15 chr9:596600-610800 Weak transcription Cortex derived primary cultured neurospheres brain
16 chr9:596800-604400 Weak transcription Left Ventricle heart
17 chr9:599000-603000 Weak transcription Fetal Intestine Large intestine
18 chr9:599600-600400 Enhancers Fetal Heart heart

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