Variant report

Variant rs13259412
Chromosome Location chr8:51552744-51552745
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:51545000-51553800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr8:51550600-51555600 Enhancers HUVEC blood vessel
3 chr8:51552000-51554000 Enhancers Primary B cells from cord blood blood
4 chr8:51552400-51554000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr8:51552400-51554200 Enhancers Hela-S3 cervix
6 chr8:51552400-51554600 Enhancers HUES64 Cell Line embryonic stem cell
7 chr8:51552400-51556000 Enhancers Cortex derived primary cultured neurospheres brain
8 chr8:51552600-51553000 Flanking Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr8:51552600-51553400 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr8:51552600-51553400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr8:51552600-51553800 Enhancers Pancreatic Islets Pancreatic Islet
12 chr8:51552600-51554200 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr8:51552600-51554200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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