Variant report

Variant rs28688827
Chromosome Location chr4:26994513-26994514
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:79 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:26966600-26994600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr4:26975800-27003200 Weak transcription Aorta Aorta
3 chr4:26978000-26994600 Weak transcription Fetal Stomach stomach
4 chr4:26978400-27019200 Weak transcription Fetal Intestine Small intestine
5 chr4:26980400-26994800 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr4:26980400-27019400 Weak transcription Left Ventricle heart
7 chr4:26985400-27019400 Weak transcription Esophagus oesophagus
8 chr4:26986400-26994600 Weak transcription Small Intestine intestine
9 chr4:26988400-26994600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr4:26988400-26998000 Weak transcription Dnd41 blood
11 chr4:26989000-27010000 Weak transcription Thymus Thymus
12 chr4:26989000-27010400 Weak transcription Fetal Thymus thymus
13 chr4:26989200-26994600 Weak transcription Pancreas Pancrea
14 chr4:26989400-26994600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr4:26989400-26996000 Weak transcription iPS-18 Cell Line embryonic stem cell
16 chr4:26989400-26997000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
17 chr4:26989400-27024800 Weak transcription Psoas Muscle Psoas
18 chr4:26989600-27027000 Weak transcription HepG2 liver
19 chr4:26993200-26995000 Enhancers Cortex derived primary cultured neurospheres brain
20 chr4:26993200-26996800 Enhancers Fetal Lung lung
21 chr4:26993200-26997000 Enhancers Primary T killer memory cells from peripheral blood blood
22 chr4:26993200-26997200 Enhancers Primary T killer naive cells fromperipheralblood blood
23 chr4:26993400-26995200 Weak transcription Brain Germinal Matrix brain
24 chr4:26993400-26995400 Enhancers Primary hematopoietic stem cells short term culture blood
25 chr4:26993400-26996000 Enhancers Primary T helper 17 cells PMA-I stimulated --
26 chr4:26993400-26996200 Enhancers Primary T regulatory cells fromperipheralblood blood
27 chr4:26993400-26996800 Enhancers Colon Smooth Muscle Colon
28 chr4:26993400-26997000 Enhancers Primary T helper memory cells from peripheral blood 2 blood
29 chr4:26993400-26997000 Enhancers Brain Hippocampus Middle brain
30 chr4:26993400-26997200 Enhancers Primary T helper memory cells from peripheral blood 1 blood
31 chr4:26993400-26997200 Enhancers Primary T helper cells fromperipheralblood blood
32 chr4:26993400-26997200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
33 chr4:26993400-26997400 Enhancers Primary T helper naive cells fromperipheralblood blood
34 chr4:26993400-26997800 Enhancers Primary T cells from cord blood blood
35 chr4:26993600-26994600 Weak transcription Ovary ovary
36 chr4:26993800-26994600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
37 chr4:26993800-26996600 Enhancers Brain Anterior Caudate brain
38 chr4:26994000-26994600 Enhancers Primary hematopoietic stem cells blood
39 chr4:26994000-26994800 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
40 chr4:26994000-26994800 Enhancers Duodenum Mucosa Duodenum
41 chr4:26994000-26995000 Enhancers Primary monocytes fromperipheralblood blood
42 chr4:26994000-26995000 Enhancers Fetal Muscle Leg muscle
43 chr4:26994000-26995200 Flanking Active TSS Primary B cells from peripheral blood blood
44 chr4:26994000-26995400 Enhancers Muscle Satellite Cultured Cells --
45 chr4:26994000-26995400 Enhancers Rectal Smooth Muscle rectum
46 chr4:26994000-26995600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
47 chr4:26994000-26995600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
48 chr4:26994000-26995600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
49 chr4:26994000-26995600 Enhancers Osteobl bone
50 chr4:26994000-26996400 Enhancers Brain Angular Gyrus brain

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