Variant report

Variant rs2305489
Chromosome Location chr4:997488-997489
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:58 , 50 per page) page: 1 2
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:991600-1002800 Weak transcription Right Atrium heart
2 chr4:993000-997800 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr4:995200-997800 Flanking Bivalent TSS/Enh iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:995400-997600 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
5 chr4:995600-997600 Enhancers Pancreas Pancrea
6 chr4:995800-997600 Bivalent/Poised TSS ES-I3 Cell Line embryonic stem cell
7 chr4:995800-997600 Bivalent/Poised TSS H9 Cell Line embryonic stem cell
8 chr4:995800-997600 Bivalent/Poised TSS HUES64 Cell Line embryonic stem cell
9 chr4:995800-997600 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
10 chr4:995800-997600 Bivalent Enhancer Primary T helper memory cells from peripheral blood 1 blood
11 chr4:995800-997600 Bivalent Enhancer Primary T cells effector/memory enriched fromperipheralblood blood
12 chr4:995800-997600 Bivalent Enhancer Primary T killer naive cells fromperipheralblood blood
13 chr4:995800-997600 Bivalent Enhancer Placenta Placenta
14 chr4:995800-997800 Bivalent Enhancer Adipose Nuclei Adipose
15 chr4:995800-998000 Bivalent Enhancer Primary T helper cells PMA-I stimulated --
16 chr4:995800-999400 Enhancers Fetal Heart heart
17 chr4:996000-997600 Bivalent/Poised TSS iPS-18 Cell Line embryonic stem cell
18 chr4:996000-997600 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
19 chr4:996000-997600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin03 Skin
20 chr4:996000-997800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
21 chr4:996200-997800 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
22 chr4:996200-998000 Bivalent Enhancer Spleen Spleen
23 chr4:996400-997600 Bivalent Enhancer Primary T helper cells fromperipheralblood blood
24 chr4:996400-997600 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Male --
25 chr4:996400-997600 Bivalent Enhancer Lung lung
26 chr4:996400-997800 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --
27 chr4:996400-998000 Bivalent Enhancer Stomach Smooth Muscle stomach
28 chr4:996600-997600 Enhancers Brain Inferior Temporal Lobe brain
29 chr4:996600-997800 Bivalent Enhancer Primary T helper naive cells from peripheral blood blood
30 chr4:996600-997800 Bivalent Enhancer Brain Germinal Matrix brain
31 chr4:996600-997800 Bivalent Enhancer Fetal Muscle Leg muscle
32 chr4:996600-998000 Bivalent Enhancer Primary T regulatory cells fromperipheralblood blood
33 chr4:996800-997800 Bivalent Enhancer Colonic Mucosa Colon
34 chr4:996800-1002800 Weak transcription Gastric stomach
35 chr4:997200-997600 Flanking Bivalent TSS/Enh H1 Cell Line embryonic stem cell
36 chr4:997200-997600 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
37 chr4:997200-997600 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
38 chr4:997200-997600 Bivalent Enhancer Fetal Intestine Large intestine
39 chr4:997200-997600 Bivalent Enhancer Fetal Intestine Small intestine
40 chr4:997200-997600 Bivalent Enhancer Right Ventricle heart
41 chr4:997200-997800 Bivalent Enhancer Primary T cells fromperipheralblood blood
42 chr4:997200-997800 Bivalent Enhancer Left Ventricle heart
43 chr4:997200-997800 Bivalent Enhancer Ovary ovary
44 chr4:997400-997600 Flanking Bivalent TSS/Enh iPS DF 6.9 Cell Line embryonic stem cell
45 chr4:997400-997600 Bivalent Enhancer Primary T helper memory cells from peripheral blood 2 blood
46 chr4:997400-997600 Bivalent Enhancer Primary Natural Killer cells fromperipheralblood blood
47 chr4:997400-997600 Bivalent Enhancer Primary T killer memory cells from peripheral blood blood
48 chr4:997400-997600 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin01 Skin
49 chr4:997400-997600 Bivalent Enhancer Brain Dorsolateral Prefrontal Cortex brain
50 chr4:997400-997600 Bivalent Enhancer Duodenum Mucosa Duodenum

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