Variant report

Variant rs564770700
Chromosome Location chr6:70591881-70591882
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:70588800-70597800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr6:70590600-70592200 Active TSS GM12878-XiMat blood
3 chr6:70590800-70592000 Enhancers Fetal Lung lung
4 chr6:70591400-70592000 Enhancers Monocytes-CD14+_RO01746 blood
5 chr6:70591400-70592200 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr6:70591400-70592400 Enhancers Primary hematopoietic stem cells short term culture blood
7 chr6:70591600-70593400 Enhancers Fetal Heart heart
8 chr6:70591800-70592000 Active TSS Primary B cells from peripheral blood blood
9 chr6:70591800-70592000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr6:70591800-70592000 Enhancers Psoas Muscle Psoas
11 chr6:70591800-70592400 Active TSS Primary B cells from cord blood blood
12 chr6:70591800-70592600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr6:70591800-70592600 Bivalent Enhancer Primary hematopoietic stem cells blood

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