The 2.0 version of rSNPBase

Variant report

Variant rs58471713
Chromosome Location chr18:11841658-11841659
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:11825400-11849800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr18:11830800-11849000 Weak transcription A549 lung
3 chr18:11831800-11842600 Weak transcription H1 Cell Line embryonic stem cell
4 chr18:11837400-11849200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr18:11837400-11849200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr18:11840400-11849200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr18:11840800-11845200 Weak transcription K562 blood
8 chr18:11841000-11841800 Enhancers HepG2 liver
9 chr18:11841000-11849600 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr18:11841000-11849800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr18:11841200-11849400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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Last update: Aug 31, 2015