Variant report

Variant rs201029374
Chromosome Location chr2:56410941-56410942
allele -/A
Outlinks Ensembl   UCSC
Chromatin state (count:107 , 50 per page) page: 1 2 3
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:56409200-56411000 Enhancers Placenta Placenta
2 chr2:56409400-56411200 Weak transcription Fetal Heart heart
3 chr2:56409800-56411000 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr2:56410000-56411000 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
5 chr2:56410200-56411000 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
6 chr2:56410400-56412800 Bivalent/Poised TSS hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr2:56410600-56411000 Bivalent Enhancer Fetal Thymus thymus
8 chr2:56410600-56411200 Bivalent Enhancer Primary monocytes fromperipheralblood blood
9 chr2:56410600-56411200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr2:56410600-56411200 Active TSS Ganglion Eminence derived primary cultured neurospheres brain
11 chr2:56410600-56411200 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
12 chr2:56410600-56411200 Active TSS Right Ventricle heart
13 chr2:56410600-56411400 Bivalent Enhancer Stomach Mucosa stomach
14 chr2:56410600-56411600 Active TSS Lung lung
15 chr2:56410600-56411600 Flanking Bivalent TSS/Enh Skeletal Muscle Male skeletal muscle
16 chr2:56410600-56411800 Bivalent Enhancer Primary T cells fromperipheralblood blood
17 chr2:56410600-56411800 Enhancers Fetal Brain Male brain
18 chr2:56410600-56411800 Active TSS Fetal Brain Female brain
19 chr2:56410600-56411800 Bivalent/Poised TSS Fetal Stomach stomach
20 chr2:56410600-56412000 Bivalent/Poised TSS HepG2 liver
21 chr2:56410600-56412000 Flanking Bivalent TSS/Enh Monocytes-CD14+_RO01746 blood
22 chr2:56410600-56412600 Bivalent Enhancer Primary B cells from peripheral blood blood
23 chr2:56410600-56412600 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
24 chr2:56410600-56412800 Active TSS HSMM muscle
25 chr2:56410600-56413000 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
26 chr2:56410600-56413000 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
27 chr2:56410600-56413000 Active TSS Muscle Satellite Cultured Cells --
28 chr2:56410600-56413000 Active TSS HSMMtube muscle
29 chr2:56410600-56413200 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
30 chr2:56410600-56413200 Active TSS Brain Angular Gyrus brain
31 chr2:56410600-56413400 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
32 chr2:56410600-56413400 Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
33 chr2:56410600-56413400 Active TSS Brain Hippocampus Middle brain
34 chr2:56410600-56413400 Active TSS Brain Dorsolateral Prefrontal Cortex brain
35 chr2:56410600-56413600 Active TSS Psoas Muscle Psoas
36 chr2:56410600-56413600 Active TSS Right Atrium heart
37 chr2:56410800-56411000 Bivalent/Poised TSS H9 Derived Neuron Cultured Cells ES cell derived
38 chr2:56410800-56411000 Bivalent/Poised TSS Primary B cells from cord blood blood
39 chr2:56410800-56411000 Bivalent/Poised TSS Primary T helper cells PMA-I stimulated --
40 chr2:56410800-56411000 Bivalent/Poised TSS Primary T cells effector/memory enriched fromperipheralblood blood
41 chr2:56410800-56411000 Bivalent/Poised TSS Cortex derived primary cultured neurospheres brain
42 chr2:56410800-56411000 Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
43 chr2:56410800-56411000 Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
44 chr2:56410800-56411000 Bivalent/Poised TSS Primary mononuclear cells fromperipheralblood Blood
45 chr2:56410800-56411000 Active TSS Rectal Mucosa Donor 29 rectum
46 chr2:56410800-56411000 Active TSS Skeletal Muscle Female skeletal muscle
47 chr2:56410800-56411000 Active TSS Stomach Smooth Muscle stomach
48 chr2:56410800-56411000 Bivalent/Poised TSS Thymus Thymus
49 chr2:56410800-56411000 Active TSS HMEC breast
50 chr2:56410800-56411000 Active TSS NH-A brain

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