Variant report

Variant rs11145957
Chromosome Location chr9:139863547-139863548
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:39 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139859200-139864800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr9:139859400-139867800 Weak transcription A549 lung
3 chr9:139859600-139869600 Weak transcription Gastric stomach
4 chr9:139860800-139865000 Weak transcription HSMMtube muscle
5 chr9:139860800-139869000 Weak transcription Esophagus oesophagus
6 chr9:139860800-139869600 Weak transcription Liver Liver
7 chr9:139861000-139864000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr9:139861000-139864400 Weak transcription Thymus Thymus
9 chr9:139861000-139865000 Weak transcription Spleen Spleen
10 chr9:139861000-139867200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:139861000-139867400 Weak transcription Hela-S3 cervix
12 chr9:139861000-139869000 Weak transcription Left Ventricle heart
13 chr9:139861000-139869200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr9:139861000-139871200 Weak transcription iPS-15b Cell Line embryonic stem cell
15 chr9:139861000-139871800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
16 chr9:139861200-139864600 Weak transcription Fetal Thymus thymus
17 chr9:139861200-139865000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
18 chr9:139861200-139869600 Weak transcription Brain Angular Gyrus brain
19 chr9:139861200-139869600 Weak transcription Brain Inferior Temporal Lobe brain
20 chr9:139861800-139869400 Weak transcription Brain Hippocampus Middle brain
21 chr9:139862000-139864000 Weak transcription Monocytes-CD14+_RO01746 blood
22 chr9:139862000-139865000 Weak transcription Primary T helper 17 cells PMA-I stimulated --
23 chr9:139862000-139867400 Weak transcription Primary Natural Killer cells fromperipheralblood blood
24 chr9:139862000-139867600 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
25 chr9:139862200-139864400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
26 chr9:139862600-139863800 Enhancers Right Ventricle heart
27 chr9:139862600-139864200 Enhancers Fetal Adrenal Gland Adrenal Gland
28 chr9:139862600-139867000 Enhancers Placenta Placenta
29 chr9:139862800-139865600 Bivalent Enhancer Fetal Muscle Trunk muscle
30 chr9:139863000-139863600 Bivalent Enhancer Fetal Stomach stomach
31 chr9:139863000-139863800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
32 chr9:139863000-139867600 Weak transcription Primary T cells fromperipheralblood blood
33 chr9:139863200-139865600 Enhancers Fetal Lung lung
34 chr9:139863400-139863600 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin01 Skin
35 chr9:139863400-139863600 Bivalent Enhancer Stomach Smooth Muscle stomach
36 chr9:139863400-139863800 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
37 chr9:139863400-139863800 Flanking Bivalent TSS/Enh HepG2 liver
38 chr9:139863400-139864200 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
39 chr9:139863400-139865000 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin

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