Variant report

Variant rs73455552
Chromosome Location chr11:36621858-36621859
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:36616600-36640400 Weak transcription Esophagus oesophagus
2 chr11:36616600-36657000 Weak transcription Left Ventricle heart
3 chr11:36616800-36639600 Weak transcription Aorta Aorta
4 chr11:36617000-36622200 Weak transcription Monocytes-CD14+_RO01746 blood
5 chr11:36617200-36622000 Weak transcription Primary hematopoietic stem cells blood
6 chr11:36617200-36626800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:36617200-36630000 Weak transcription HSMMtube muscle
8 chr11:36617200-36640000 Weak transcription Fetal Stomach stomach
9 chr11:36617400-36632400 Weak transcription Stomach Smooth Muscle stomach
10 chr11:36617600-36622000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr11:36618000-36623400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
12 chr11:36618000-36640400 Weak transcription Primary T cells from cord blood blood
13 chr11:36618400-36622000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr11:36620200-36622200 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr11:36621000-36635400 Enhancers Dnd41 blood
16 chr11:36621800-36622000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr11:36621800-36622000 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
18 chr11:36621800-36622200 Flanking Active TSS Fetal Thymus thymus
19 chr11:36621800-36622200 Flanking Active TSS Thymus Thymus

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