Variant report

Variant rs546684465
Chromosome Location chr2:37947757-37947758
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:37941800-37948400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr2:37944200-37948000 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr2:37946600-37948200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr2:37946600-37948200 Enhancers K562 blood
5 chr2:37946800-37949000 Enhancers Muscle Satellite Cultured Cells --
6 chr2:37947200-37948800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr2:37947200-37949800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr2:37947400-37949000 Enhancers Osteobl bone
9 chr2:37947600-37948000 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr2:37947600-37948400 Flanking Active TSS NHDF-Ad bronchial
11 chr2:37947600-37948600 Enhancers Fetal Thymus thymus
12 chr2:37947600-37948800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr2:37947600-37948800 Enhancers Fetal Brain Female brain
14 chr2:37947600-37949000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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