Variant report

Variant rs562549058
Chromosome Location chr10:44296955-44296956
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44286000-44302600 Weak transcription Aorta Aorta
2 chr10:44290000-44300600 Weak transcription Osteobl bone
3 chr10:44290000-44303200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr10:44292600-44304800 Weak transcription Fetal Muscle Leg muscle
5 chr10:44293400-44300800 Weak transcription Right Atrium heart
6 chr10:44293400-44304600 Weak transcription Ovary ovary
7 chr10:44294800-44299400 Weak transcription Right Ventricle heart
8 chr10:44295000-44300600 Weak transcription NHDF-Ad bronchial
9 chr10:44295000-44311000 Weak transcription Left Ventricle heart
10 chr10:44296000-44300000 Weak transcription Fetal Lung lung
11 chr10:44296400-44297200 Enhancers Primary T cells from cord blood blood
12 chr10:44296400-44297400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr10:44296600-44297200 Enhancers Primary T helper naive cells fromperipheralblood blood
14 chr10:44296600-44297200 Enhancers Fetal Stomach stomach
15 chr10:44296600-44298200 Enhancers Adipose Nuclei Adipose
16 chr10:44296800-44297000 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
17 chr10:44296800-44297000 Enhancers Primary T helper 17 cells PMA-I stimulated --
18 chr10:44296800-44297400 Enhancers Placenta Placenta

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