The 2.0 version of rSNPBase

Variant report

Variant rs12457247
Chromosome Location chr18:11768762-11768763
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:11752800-11774000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr18:11753000-11774800 Weak transcription Stomach Smooth Muscle stomach
3 chr18:11753000-11775400 Weak transcription Gastric stomach
4 chr18:11756600-11769200 Weak transcription Fetal Brain Female brain
5 chr18:11758400-11785600 Weak transcription Brain Anterior Caudate brain
6 chr18:11763400-11780400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr18:11765800-11768800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
8 chr18:11767200-11769000 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr18:11767600-11785400 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr18:11767600-11789000 Weak transcription Esophagus oesophagus
11 chr18:11767800-11769400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr18:11767800-11771400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
13 chr18:11767800-11783800 Weak transcription H9 Cell Line embryonic stem cell
14 chr18:11767800-11784000 Weak transcription Aorta Aorta
15 chr18:11768200-11772800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr18:11768400-11769400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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Last update: Aug 31, 2015