Variant report

Variant rs10105902
Chromosome Location chr8:118786029-118786030
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:118751400-118805400 Weak transcription NHLF lung
2 chr8:118777800-118802200 Weak transcription NHDF-Ad bronchial
3 chr8:118779800-118801200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr8:118781400-118801200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr8:118782200-118787000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:118783400-118786400 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr8:118784000-118804200 Weak transcription NH-A brain
8 chr8:118784200-118801400 Weak transcription Osteobl bone
9 chr8:118784600-118787600 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr8:118784600-118801600 Weak transcription Aorta Aorta
11 chr8:118785200-118786800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr8:118785200-118787000 Enhancers Muscle Satellite Cultured Cells --
13 chr8:118785400-118789200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr8:118785400-118800800 Weak transcription HSMM muscle
15 chr8:118785600-118787000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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