Variant report

Variant rs11033708
Chromosome Location chr11:36622802-36622803
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr11:36617200-36626800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr11:36617200-36630000 Weak transcription HSMMtube muscle
6 chr11:36617200-36640000 Weak transcription Fetal Stomach stomach
7 chr11:36617400-36632400 Weak transcription Stomach Smooth Muscle stomach
8 chr11:36618000-36623400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr11:36618000-36640400 Weak transcription Primary T cells from cord blood blood
10 chr11:36621000-36635400 Enhancers Dnd41 blood
11 chr11:36622000-36625000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr11:36622000-36625600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr11:36622200-36624200 Active TSS Thymus Thymus
14 chr11:36622400-36624000 Enhancers Primary monocytes fromperipheralblood blood
15 chr11:36622600-36623000 Flanking Active TSS Primary hematopoietic stem cells blood
16 chr11:36622600-36623200 Active TSS Fetal Thymus thymus
17 chr11:36622600-36623200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
18 chr11:36622800-36625600 Enhancers Primary hematopoietic stem cells short term culture blood

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