Variant report

Variant rs552168187
Chromosome Location chr11:86930814-86930815
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:86906000-86931000 Weak transcription Fetal Lung lung
2 chr11:86915400-86942000 Weak transcription HepG2 liver
3 chr11:86916000-86931000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr11:86924800-86934800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr11:86926600-86935200 Weak transcription Fetal Stomach stomach
6 chr11:86926800-86934600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr11:86927000-86933800 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr11:86929600-86942000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr11:86930200-86931000 Enhancers GM12878-XiMat blood
10 chr11:86930200-86932600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr11:86930400-86931800 Enhancers Colon Smooth Muscle Colon
12 chr11:86930600-86931200 Enhancers Osteobl bone
13 chr11:86930800-86934000 Weak transcription iPS-18 Cell Line embryonic stem cell

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