Variant report

Variant rs11068336
Chromosome Location chr12:117539486-117539487
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:117537600-117540000 Enhancers Primary monocytes fromperipheralblood blood
2 chr12:117537600-117540000 Weak transcription Left Ventricle heart
3 chr12:117537600-117540600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr12:117537600-117556400 Weak transcription Right Atrium heart
5 chr12:117537800-117539800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr12:117537800-117539800 Enhancers Monocytes-CD14+_RO01746 blood
7 chr12:117537800-117540200 Enhancers A549 lung
8 chr12:117537800-117540400 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr12:117537800-117543200 Weak transcription Dnd41 blood
10 chr12:117538200-117540400 Enhancers Fetal Thymus thymus
11 chr12:117538800-117539800 Bivalent Enhancer Adipose Nuclei Adipose
12 chr12:117538800-117540800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr12:117538800-117540800 Bivalent Enhancer Fetal Muscle Leg muscle
14 chr12:117538800-117549200 Weak transcription Pancreas Pancrea
15 chr12:117539000-117539800 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
16 chr12:117539200-117539600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
17 chr12:117539200-117540000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
18 chr12:117539200-117540200 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
19 chr12:117539400-117539600 Enhancers Primary neutrophils fromperipheralblood blood
20 chr12:117539400-117539600 Flanking Active TSS HepG2 liver
21 chr12:117539400-117540400 Bivalent Enhancer H9 Derived Neuron Cultured Cells ES cell derived
22 chr12:117539400-117540800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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