Variant report

Variant rs34578251
Chromosome Location chr7:17560348-17560349
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17553200-17560600 Weak transcription Liver Liver
2 chr7:17557200-17560400 Weak transcription NHDF-Ad bronchial
3 chr7:17557200-17563600 Weak transcription NHLF lung
4 chr7:17559400-17560600 Enhancers Muscle Satellite Cultured Cells --
5 chr7:17559600-17561000 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr7:17559600-17569200 Weak transcription Aorta Aorta
7 chr7:17560000-17560800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr7:17560000-17562000 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr7:17560000-17562000 Enhancers Osteobl bone
10 chr7:17560000-17562400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr7:17560000-17562400 Enhancers HSMM muscle
12 chr7:17560200-17560600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr7:17560200-17560800 Enhancers HUVEC blood vessel
14 chr7:17560200-17561000 Enhancers Primary T cells from cord blood blood
15 chr7:17560200-17561800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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