Variant report

Variant rs2853550
Chromosome Location chr2:113587121-113587122
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113582200-113588800 Weak transcription Lung lung
2 chr2:113582400-113592000 Weak transcription NH-A brain
3 chr2:113582800-113589400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr2:113583000-113587200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:113583000-113592200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:113583600-113587200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr2:113583600-113587200 Weak transcription HMEC breast
8 chr2:113583600-113591200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr2:113583600-113592000 Weak transcription Osteobl bone
10 chr2:113585200-113587200 Weak transcription Primary monocytes fromperipheralblood blood
11 chr2:113585400-113587400 Weak transcription Monocytes-CD14+_RO01746 blood
12 chr2:113585600-113587400 Enhancers K562 blood
13 chr2:113586400-113588800 Genic enhancers Primary hematopoietic stem cells blood
14 chr2:113586600-113587600 Genic enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr2:113586800-113588000 Genic enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr2:113586800-113588200 Strong transcription Primary neutrophils fromperipheralblood blood
17 chr2:113586800-113588800 Genic enhancers Primary hematopoietic stem cells short term culture blood
18 chr2:113586800-113589000 Weak transcription Pancreas Pancrea
19 chr2:113587000-113587200 Enhancers Fetal Intestine Small intestine
20 chr2:113587000-113589000 Weak transcription Primary B cells from cord blood blood
21 chr2:113587000-113589000 Strong transcription NHEK skin
22 chr2:113587000-113589600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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