Variant report

Variant rs57472392
Chromosome Location chr6:145978241-145978242
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145950800-145990600 Weak transcription Primary B cells from cord blood blood
2 chr6:145951000-146003000 Weak transcription Thymus Thymus
3 chr6:145951400-146003000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr6:145952200-145983200 Weak transcription Primary T cells from cord blood blood
5 chr6:145960200-145978800 Weak transcription Fetal Heart heart
6 chr6:145973400-145978800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr6:145973600-145990600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr6:145974200-146002800 Weak transcription Liver Liver
9 chr6:145974800-146003600 Weak transcription Primary T helper naive cells fromperipheralblood blood
10 chr6:145976000-145984400 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr6:145976600-145978600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr6:145976600-145984200 Weak transcription Primary hematopoietic stem cells blood

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