Variant report

Variant rs61818299
Chromosome Location chr1:215259486-215259487
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:215254800-215260000 Active TSS Fetal Brain Female brain
2 chr1:215257200-215259800 Weak transcription Gastric stomach
3 chr1:215257400-215260600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:215257800-215260800 Weak transcription Muscle Satellite Cultured Cells --
5 chr1:215258200-215277600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr1:215258400-215261000 Weak transcription Osteobl bone
7 chr1:215258400-215265000 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr1:215258400-215267400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:215258400-215277600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:215258600-215259600 Weak transcription Fetal Brain Male brain
11 chr1:215258800-215261200 Weak transcription NHLF lung
12 chr1:215259000-215259600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr1:215259200-215259800 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr1:215259400-215260000 Strong transcription NHDF-Ad bronchial

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