Variant report

Variant rs9690738
Chromosome Location chr7:69406143-69406144
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:69387600-69409400 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr7:69391800-69417000 Weak transcription Primary B cells from cord blood blood
3 chr7:69402000-69406800 Enhancers Fetal Thymus thymus
4 chr7:69403800-69409000 Weak transcription Fetal Heart heart
5 chr7:69404400-69407200 Enhancers Primary T cells from cord blood blood
6 chr7:69404600-69427800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr7:69404800-69409600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr7:69405800-69406400 Enhancers Brain Hippocampus Middle brain
9 chr7:69406000-69406200 Enhancers Psoas Muscle Psoas
10 chr7:69406000-69406400 Enhancers Cortex derived primary cultured neurospheres brain
11 chr7:69406000-69406400 Enhancers Adipose Nuclei Adipose
12 chr7:69406000-69406400 Enhancers Brain Anterior Caudate brain
13 chr7:69406000-69406400 Enhancers Colon Smooth Muscle Colon
14 chr7:69406000-69406600 Enhancers GM12878-XiMat blood
15 chr7:69406000-69406800 Enhancers Primary B cells from peripheral blood blood
16 chr7:69406000-69406800 Enhancers Thymus Thymus
17 chr7:69406000-69408800 Enhancers Fetal Brain Male brain
18 chr7:69406000-69409000 Enhancers Fetal Brain Female brain

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