Variant report

Variant rs10870117
Chromosome Location chr9:139637087-139637088
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:48 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139634800-139638000 Enhancers Fetal Heart heart
2 chr9:139635000-139637400 Flanking Active TSS Primary B cells from peripheral blood blood
3 chr9:139635000-139637800 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
4 chr9:139635200-139638000 Bivalent Enhancer Placenta Placenta
5 chr9:139635200-139638000 Enhancers Pancreas Pancrea
6 chr9:139635200-139638200 Enhancers Gastric stomach
7 chr9:139635400-139637200 Bivalent Enhancer Adipose Nuclei Adipose
8 chr9:139635400-139637600 Bivalent Enhancer Fetal Stomach stomach
9 chr9:139635400-139637600 Enhancers Lung lung
10 chr9:139635400-139637600 Flanking Bivalent TSS/Enh HepG2 liver
11 chr9:139635400-139637800 Bivalent Enhancer Stomach Mucosa stomach
12 chr9:139635600-139637800 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
13 chr9:139635600-139638000 Enhancers H1 Cell Line embryonic stem cell
14 chr9:139635600-139638400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
15 chr9:139636000-139637200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr9:139636000-139637800 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
17 chr9:139636000-139638000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
18 chr9:139636200-139637400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr9:139636200-139637400 Weak transcription Liver Liver
20 chr9:139636200-139637600 Enhancers Primary hematopoietic stem cells blood
21 chr9:139636200-139640600 Active TSS Left Ventricle heart
22 chr9:139636400-139637200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
23 chr9:139636400-139637200 Active TSS Right Ventricle heart
24 chr9:139636400-139637400 Enhancers Primary T helper memory cells from peripheral blood 1 blood
25 chr9:139636400-139637400 Bivalent Enhancer Fetal Thymus thymus
26 chr9:139636400-139637600 Bivalent Enhancer GM12878-XiMat blood
27 chr9:139636400-139637800 Bivalent Enhancer Colonic Mucosa Colon
28 chr9:139636400-139639800 Weak transcription K562 blood
29 chr9:139636600-139637400 Flanking Bivalent TSS/Enh Fetal Intestine Large intestine
30 chr9:139636600-139637600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
31 chr9:139636600-139639200 Enhancers Primary hematopoietic stem cells short term culture blood
32 chr9:139636600-139641200 Enhancers Spleen Spleen
33 chr9:139636800-139637200 Bivalent Enhancer Fetal Intestine Small intestine
34 chr9:139636800-139637400 Enhancers Primary T cells effector/memory enriched fromperipheralblood blood
35 chr9:139636800-139637600 Enhancers Primary T helper cells fromperipheralblood blood
36 chr9:139637000-139637200 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle
37 chr9:139637000-139637400 Enhancers Primary T helper cells PMA-I stimulated --
38 chr9:139637000-139637400 Bivalent Enhancer Primary T regulatory cells fromperipheralblood blood
39 chr9:139637000-139637400 Flanking Bivalent TSS/Enh Fetal Muscle Leg muscle
40 chr9:139637000-139637600 Weak transcription ES-WA7 Cell Line embryonic stem cell
41 chr9:139637000-139637600 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
42 chr9:139637000-139637600 Bivalent Enhancer Primary T cells fromperipheralblood blood
43 chr9:139637000-139637600 Enhancers Primary T helper naive cells fromperipheralblood blood
44 chr9:139637000-139637600 Bivalent Enhancer Esophagus oesophagus
45 chr9:139637000-139637800 Enhancers Primary Natural Killer cells fromperipheralblood blood
46 chr9:139637000-139638000 Enhancers Primary B cells from cord blood blood
47 chr9:139637000-139638200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
48 chr9:139637000-139639200 Weak transcription Right Atrium heart

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