Variant report

Variant rs74106272
Chromosome Location chr12:83102026-83102027
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:58 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:83082200-83102200 Weak transcription Lung lung
2 chr12:83082800-83102200 Weak transcription Pancreas Pancrea
3 chr12:83086000-83102200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr12:83086600-83122200 Weak transcription Fetal Muscle Trunk muscle
5 chr12:83087200-83105600 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr12:83087400-83106400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr12:83092800-83102200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr12:83093200-83122400 Weak transcription Gastric stomach
9 chr12:83095400-83106600 Weak transcription Fetal Intestine Large intestine
10 chr12:83096000-83105800 Weak transcription Fetal Intestine Small intestine
11 chr12:83098000-83121200 Weak transcription Primary mononuclear cells fromperipheralblood Blood
12 chr12:83098800-83106800 Strong transcription Monocytes-CD14+_RO01746 blood
13 chr12:83099200-83122400 Weak transcription Esophagus oesophagus
14 chr12:83099400-83102200 Enhancers Brain Substantia Nigra brain
15 chr12:83099400-83103800 Weak transcription Primary monocytes fromperipheralblood blood
16 chr12:83100400-83102200 Enhancers Brain Anterior Caudate brain
17 chr12:83100400-83103200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
18 chr12:83100600-83102200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
19 chr12:83100600-83102400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
20 chr12:83100600-83102800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
21 chr12:83100600-83103000 Enhancers HUES48 Cell Line embryonic stem cell
22 chr12:83100800-83102200 Enhancers Brain Hippocampus Middle brain
23 chr12:83100800-83102200 Enhancers Colon Smooth Muscle Colon
24 chr12:83100800-83102800 Enhancers Fetal Heart heart
25 chr12:83101000-83102800 Enhancers Cortex derived primary cultured neurospheres brain
26 chr12:83101000-83104800 Enhancers Rectal Smooth Muscle rectum
27 chr12:83101200-83102400 Enhancers Brain Inferior Temporal Lobe brain
28 chr12:83101200-83102600 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
29 chr12:83101200-83102800 Enhancers Fetal Muscle Leg muscle
30 chr12:83101200-83102800 Enhancers Placenta Amnion Placenta Amnion
31 chr12:83101200-83103000 Enhancers Fetal Stomach stomach
32 chr12:83101400-83102400 Enhancers Fetal Kidney kidney
33 chr12:83101400-83102600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
34 chr12:83101400-83102800 Enhancers H9 Cell Line embryonic stem cell
35 chr12:83101400-83102800 Active TSS Fetal Brain Male brain
36 chr12:83101400-83102800 Enhancers Ovary ovary
37 chr12:83101400-83102800 Enhancers GM12878-XiMat blood
38 chr12:83101600-83102400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
39 chr12:83101600-83102400 Weak transcription Duodenum Smooth Muscle Duodenum
40 chr12:83101600-83102800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
41 chr12:83101600-83102800 Enhancers Fetal Lung lung
42 chr12:83101600-83103200 Enhancers iPS-18 Cell Line embryonic stem cell
43 chr12:83101800-83102400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
44 chr12:83101800-83102600 Enhancers ES-WA7 Cell Line embryonic stem cell
45 chr12:83101800-83102600 Enhancers Brain Angular Gyrus brain
46 chr12:83101800-83102800 Enhancers HUES6 Cell Line embryonic stem cell
47 chr12:83101800-83103400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
48 chr12:83102000-83102200 Flanking Active TSS Brain Dorsolateral Prefrontal Cortex brain
49 chr12:83102000-83102400 Flanking Active TSS Brain Cingulate Gyrus brain
50 chr12:83102000-83102600 Genic enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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