Variant report

Variant rs11064621
Chromosome Location chr12:1077031-1077032
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:1063200-1090400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr12:1068000-1097600 Weak transcription Stomach Smooth Muscle stomach
3 chr12:1068000-1098600 Weak transcription Aorta Aorta
4 chr12:1068200-1086200 Weak transcription Fetal Muscle Leg muscle
5 chr12:1071000-1088600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr12:1072800-1097800 Weak transcription Pancreas Pancrea
7 chr12:1073200-1099600 Weak transcription Gastric stomach
8 chr12:1074200-1097200 Weak transcription Fetal Stomach stomach
9 chr12:1074400-1077400 Weak transcription A549 lung
10 chr12:1076200-1097600 Weak transcription Primary hematopoietic stem cells short term culture blood
11 chr12:1076400-1097600 Weak transcription Brain Angular Gyrus brain
12 chr12:1076400-1097600 Weak transcription Fetal Intestine Small intestine
13 chr12:1076800-1078000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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