Variant report

Variant nsv874895
Chromosome Location chr2:113870663-113875892
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:151 , 50 per page) page: 1 2 3 4
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113868200-113871400 Weak transcription Gastric stomach
2 chr2:113868600-113870800 Enhancers Primary hematopoietic stem cells short term culture blood
3 chr2:113868600-113875400 Enhancers Primary monocytes fromperipheralblood blood
4 chr2:113869200-113872400 Enhancers Esophagus oesophagus
5 chr2:113869400-113873000 Weak transcription Stomach Mucosa stomach
6 chr2:113869800-113871600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:113869800-113872400 Weak transcription Placenta Amnion Placenta Amnion
8 chr2:113869800-113873400 Weak transcription Primary T killer memory cells from peripheral blood blood
9 chr2:113870000-113870800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
10 chr2:113870200-113870800 Enhancers H9 Cell Line embryonic stem cell
11 chr2:113870200-113870800 Enhancers HUES48 Cell Line embryonic stem cell
12 chr2:113870200-113870800 Enhancers HUES6 Cell Line embryonic stem cell
13 chr2:113870200-113870800 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr2:113870200-113870800 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr2:113870200-113871800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr2:113870200-113873000 Weak transcription Primary hematopoietic stem cells blood
17 chr2:113870200-113873000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
18 chr2:113870200-113873200 Weak transcription Spleen Spleen
19 chr2:113870400-113870800 Enhancers iPS-18 Cell Line embryonic stem cell
20 chr2:113870400-113870800 Enhancers K562 blood
21 chr2:113870400-113871400 Weak transcription Placenta Placenta
22 chr2:113870400-113871400 Weak transcription NHEK skin
23 chr2:113870400-113872800 Weak transcription Primary Natural Killer cells fromperipheralblood blood
24 chr2:113870400-113873400 Enhancers Monocytes-CD14+_RO01746 blood
25 chr2:113870800-113871800 Weak transcription Primary hematopoietic stem cells short term culture blood
26 chr2:113870800-113872600 Enhancers Primary neutrophils fromperipheralblood blood
27 chr2:113871400-113871600 Enhancers Primary T cells from cord blood blood
28 chr2:113871400-113871600 Enhancers Primary mononuclear cells fromperipheralblood Blood
29 chr2:113871400-113871600 Enhancers Gastric stomach
30 chr2:113871400-113873600 Enhancers Placenta Placenta
31 chr2:113871400-113874800 Enhancers NHEK skin
32 chr2:113871400-113875000 Bivalent Enhancer HepG2 liver
33 chr2:113871400-113875400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
34 chr2:113871600-113874600 Weak transcription Gastric stomach
35 chr2:113871600-113875400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
36 chr2:113871800-113872800 Weak transcription Primary T cells from cord blood blood
37 chr2:113871800-113873600 Enhancers Primary hematopoietic stem cells short term culture blood
38 chr2:113871800-113873600 Enhancers HMEC breast
39 chr2:113871800-113874600 Enhancers GM12878-XiMat blood
40 chr2:113871800-113875400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
41 chr2:113872200-113873200 Bivalent Enhancer Primary B cells from cord blood blood
42 chr2:113872400-113872600 Enhancers Placenta Amnion Placenta Amnion
43 chr2:113872400-113872800 Active TSS Esophagus oesophagus
44 chr2:113872400-113873000 Enhancers Fetal Adrenal Gland Adrenal Gland
45 chr2:113872600-113872800 Flanking Active TSS Primary neutrophils fromperipheralblood blood
46 chr2:113872600-113873600 Weak transcription Placenta Amnion Placenta Amnion
47 chr2:113872600-113875600 Enhancers Primary B cells from peripheral blood blood
48 chr2:113872800-113873000 Flanking Active TSS Esophagus oesophagus
49 chr2:113872800-113873200 Enhancers Primary neutrophils fromperipheralblood blood
50 chr2:113872800-113874800 Enhancers Primary T helper cells fromperipheralblood blood

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