Variant report

Variant rs73539737
Chromosome Location chr8:11379213-11379214
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11357400-11380000 Genic enhancers Primary B cells from peripheral blood blood
2 chr8:11372200-11386000 Weak transcription Spleen Spleen
3 chr8:11374800-11381800 Weak transcription HUVEC blood vessel
4 chr8:11376200-11382000 Weak transcription Fetal Thymus thymus
5 chr8:11376600-11382200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr8:11376800-11382000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr8:11376800-11382200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr8:11377400-11379600 Genic enhancers Primary B cells from cord blood blood
9 chr8:11377400-11381200 Weak transcription GM12878-XiMat blood
10 chr8:11377400-11381800 Weak transcription Osteobl bone
11 chr8:11379200-11379400 Bivalent Enhancer Primary hematopoietic stem cells blood

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