Variant report

Variant rs11235017
Chromosome Location chr11:86933304-86933305
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:86915400-86942000 Weak transcription HepG2 liver
2 chr11:86924800-86934800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:86926600-86935200 Weak transcription Fetal Stomach stomach
4 chr11:86926800-86934600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr11:86927000-86933800 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr11:86929600-86942000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr11:86930800-86934000 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr11:86931200-86934600 Weak transcription Osteobl bone
9 chr11:86931200-86935600 Weak transcription Fetal Lung lung
10 chr11:86931600-86935000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr11:86931800-86935000 Weak transcription Colon Smooth Muscle Colon
12 chr11:86932600-86935000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr11:86933000-86942800 Weak transcription Primary B cells from cord blood blood

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