Variant report

Variant rs7849766
Chromosome Location chr9:607391-607392
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 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 chr9:592600-614400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr9:593000-608600 Weak transcription Esophagus oesophagus
5 chr9:595600-614000 Weak transcription Right Ventricle heart
6 chr9:596600-610800 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr9:602000-613400 Weak transcription A549 lung
8 chr9:603600-608400 Weak transcription Fetal Heart heart
9 chr9:603800-613200 Weak transcription Duodenum Mucosa Duodenum
10 chr9:605800-610600 Weak transcription Fetal Intestine Small intestine
11 chr9:606000-607600 Weak transcription Left Ventricle heart
12 chr9:606000-610400 Weak transcription Fetal Intestine Large intestine
13 chr9:606000-628200 Weak transcription H9 Cell Line embryonic stem cell
14 chr9:606200-608600 Weak transcription Brain Hippocampus Middle brain
15 chr9:606600-609000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr9:606800-607400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr9:606800-609000 Enhancers Breast Myoepithelial Primary Cells Breast
18 chr9:606800-609000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
19 chr9:606800-609200 Enhancers HMEC breast
20 chr9:607000-607600 Enhancers NHEK skin
21 chr9:607200-607600 Enhancers Pancreas Pancrea
22 chr9:607200-607800 Enhancers Placenta Amnion Placenta Amnion

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