Variant report

Variant rs10962098
Chromosome Location chr9:15611407-15611408
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:15587000-15620400 Weak transcription Pancreas Pancrea
2 chr9:15592800-15614000 Weak transcription Left Ventricle heart
3 chr9:15599000-15617800 Weak transcription Aorta Aorta
4 chr9:15600200-15614400 Weak transcription Gastric stomach
5 chr9:15600600-15617600 Weak transcription Fetal Stomach stomach
6 chr9:15601000-15620000 Weak transcription Ovary ovary
7 chr9:15601200-15614000 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr9:15606800-15614000 Weak transcription Fetal Lung lung
9 chr9:15607800-15614000 Weak transcription Primary hematopoietic stem cells short term culture blood
10 chr9:15608000-15618400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr9:15608400-15613800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr9:15608600-15614000 Weak transcription Fetal Thymus thymus
13 chr9:15609800-15612200 Weak transcription Stomach Smooth Muscle stomach
14 chr9:15609800-15625800 Weak transcription Brain Hippocampus Middle brain
15 chr9:15610600-15613000 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr9:15611200-15613800 Strong transcription Primary hematopoietic stem cells blood
17 chr9:15611200-15628200 Weak transcription Thymus Thymus

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