Variant report

Variant rs9458816
Chromosome Location chr6:163775360-163775361
allele A/C/G
Outlinks Ensembl   UCSC
Chromatin state (count:58 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:163767600-163776200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:163767600-163776600 Enhancers Brain Cingulate Gyrus brain
3 chr6:163768200-163775600 Weak transcription Placenta Amnion Placenta Amnion
4 chr6:163768200-163776400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr6:163768200-163776400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr6:163768400-163775800 Weak transcription Right Atrium heart
7 chr6:163768600-163775800 Weak transcription Esophagus oesophagus
8 chr6:163769000-163776000 Weak transcription Psoas Muscle Psoas
9 chr6:163770400-163775600 Weak transcription HSMM muscle
10 chr6:163770600-163775800 Weak transcription Muscle Satellite Cultured Cells --
11 chr6:163770600-163775800 Weak transcription Left Ventricle heart
12 chr6:163771200-163776000 Enhancers Primary monocytes fromperipheralblood blood
13 chr6:163772200-163778000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr6:163772200-163778600 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr6:163772400-163778800 Enhancers Placenta Placenta
16 chr6:163772600-163775800 Weak transcription Skeletal Muscle Female skeletal muscle
17 chr6:163773400-163776800 Enhancers Brain Angular Gyrus brain
18 chr6:163773400-163777600 Enhancers Fetal Muscle Leg muscle
19 chr6:163773600-163775800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
20 chr6:163773600-163778000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
21 chr6:163773800-163775800 Enhancers HUVEC blood vessel
22 chr6:163773800-163776200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
23 chr6:163774000-163775400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
24 chr6:163774000-163776000 Weak transcription HUES6 Cell Line embryonic stem cell
25 chr6:163774000-163776000 Enhancers Brain Inferior Temporal Lobe brain
26 chr6:163774200-163775800 Enhancers Brain Anterior Caudate brain
27 chr6:163774200-163776000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
28 chr6:163774400-163775400 Enhancers Brain Hippocampus Middle brain
29 chr6:163774400-163775400 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
30 chr6:163774400-163775600 Weak transcription Colon Smooth Muscle Colon
31 chr6:163774400-163775800 Weak transcription Primary hematopoietic stem cells short term culture blood
32 chr6:163774400-163776600 Enhancers Brain Substantia Nigra brain
33 chr6:163775000-163775400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
34 chr6:163775000-163775600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
35 chr6:163775000-163776000 Weak transcription Fetal Thymus thymus
36 chr6:163775000-163776000 Enhancers Skeletal Muscle Male skeletal muscle
37 chr6:163775000-163777600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
38 chr6:163775000-163777600 Enhancers Cortex derived primary cultured neurospheres brain
39 chr6:163775000-163778000 Enhancers Hela-S3 cervix
40 chr6:163775000-163778400 Enhancers Fetal Heart heart
41 chr6:163775200-163775400 Enhancers H9 Cell Line embryonic stem cell
42 chr6:163775200-163775400 Flanking Active TSS Adipose Nuclei Adipose
43 chr6:163775200-163775800 Enhancers Primary neutrophils fromperipheralblood blood
44 chr6:163775200-163776000 Weak transcription Fetal Muscle Trunk muscle
45 chr6:163775200-163776200 Enhancers NH-A brain
46 chr6:163775200-163776200 Enhancers NHDF-Ad bronchial
47 chr6:163775200-163776400 Enhancers Right Ventricle heart
48 chr6:163775200-163777200 Enhancers Fetal Lung lung
49 chr6:163775200-163777400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
50 chr6:163775200-163777400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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