Variant report

Variant rs3858283
Chromosome Location chr10:90564687-90564688
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:90560800-90569600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr10:90561000-90564800 Weak transcription Osteobl bone
3 chr10:90561000-90565000 Weak transcription NH-A brain
4 chr10:90561200-90565000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr10:90562400-90564800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr10:90564000-90564800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr10:90564000-90566000 Enhancers Hela-S3 cervix
8 chr10:90564200-90569200 Weak transcription Fetal Thymus thymus
9 chr10:90564400-90565600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr10:90564400-90566200 Enhancers Muscle Satellite Cultured Cells --
11 chr10:90564400-90566200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr10:90564600-90565400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr10:90564600-90566400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr10:90564600-90569600 Weak transcription NHEK skin
15 chr10:90564600-90569800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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