Variant report

Variant rs17347735
Chromosome Location chr9:603509-603510
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:590000-625000 Weak transcription Aorta Aorta
2 chr9:590200-621600 Weak transcription Psoas Muscle Psoas
3 chr9:592600-607200 Weak transcription Pancreas Pancrea
4 chr9:592600-614400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr9:593000-606800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr9:593000-608600 Weak transcription Esophagus oesophagus
7 chr9:593200-606800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr9:595600-614000 Weak transcription Right Ventricle heart
9 chr9:596600-605600 Weak transcription Brain Hippocampus Middle brain
10 chr9:596600-610800 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr9:596800-604400 Weak transcription Left Ventricle heart
12 chr9:600400-604600 Weak transcription Placenta Placenta
13 chr9:602000-613400 Weak transcription A549 lung
14 chr9:602600-603600 Enhancers Fetal Heart heart
15 chr9:602600-603600 Enhancers NHEK skin
16 chr9:602800-603600 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr9:602800-603600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr9:602800-603800 Enhancers Duodenum Mucosa Duodenum
19 chr9:603000-603600 Enhancers Fetal Intestine Large intestine
20 chr9:603400-603600 Enhancers Placenta Amnion Placenta Amnion
21 chr9:603400-605400 Weak transcription Fetal Intestine Small intestine

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