Variant report

Variant rs73668350
Chromosome Location chr9:139541762-139541763
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:42 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139537800-139542000 Enhancers Fetal Heart heart
2 chr9:139538000-139542000 Flanking Active TSS Primary hematopoietic stem cells short term culture blood
3 chr9:139538000-139542000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
4 chr9:139538000-139542000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr9:139538200-139541800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr9:139538200-139542200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr9:139538400-139541800 Enhancers Placenta Amnion Placenta Amnion
8 chr9:139538600-139541800 Bivalent Enhancer Fetal Thymus thymus
9 chr9:139538800-139542000 Bivalent Enhancer Placenta Placenta
10 chr9:139539000-139541800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr9:139539000-139541800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr9:139539400-139542000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr9:139539400-139548000 Weak transcription HMEC breast
14 chr9:139539600-139546400 Weak transcription Pancreas Pancrea
15 chr9:139539600-139553200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr9:139539800-139541800 Bivalent Enhancer Primary B cells from peripheral blood blood
17 chr9:139539800-139542800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
18 chr9:139540200-139541800 Flanking Bivalent TSS/Enh Fetal Adrenal Gland Adrenal Gland
19 chr9:139540600-139542000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
20 chr9:139540600-139542000 Active TSS Psoas Muscle Psoas
21 chr9:139540800-139541800 Flanking Active TSS Primary hematopoietic stem cells blood
22 chr9:139540800-139541800 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
23 chr9:139540800-139542000 Bivalent Enhancer Fetal Muscle Trunk muscle
24 chr9:139541000-139541800 Bivalent Enhancer Colonic Mucosa Colon
25 chr9:139541000-139541800 Bivalent/Poised TSS Skeletal Muscle Female skeletal muscle
26 chr9:139541000-139541800 Enhancers Spleen Spleen
27 chr9:139541000-139542000 Bivalent Enhancer Primary monocytes fromperipheralblood blood
28 chr9:139541000-139542000 Active TSS Right Atrium heart
29 chr9:139541000-139542000 Active TSS Right Ventricle heart
30 chr9:139541200-139542000 Active TSS Lung lung
31 chr9:139541200-139542000 Flanking Active TSS HUVEC blood vessel
32 chr9:139541200-139542000 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
33 chr9:139541400-139541800 Enhancers H1 Cell Line embryonic stem cell
34 chr9:139541400-139541800 Flanking Bivalent TSS/Enh Stomach Smooth Muscle stomach
35 chr9:139541400-139542000 Bivalent/Poised TSS Brain Hippocampus Middle brain
36 chr9:139541400-139542000 Enhancers K562 blood
37 chr9:139541400-139542200 Active TSS Left Ventricle heart
38 chr9:139541400-139545000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
39 chr9:139541600-139541800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
40 chr9:139541600-139541800 Bivalent Enhancer Duodenum Mucosa Duodenum
41 chr9:139541600-139542000 Flanking Active TSS Adipose Nuclei Adipose
42 chr9:139541600-139544800 Weak transcription Primary B cells from cord blood blood

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