Variant report

Variant rs4561223
Chromosome Location chr11:121592632-121592633
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:121587200-121592800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr11:121587400-121592800 Weak transcription Muscle Satellite Cultured Cells --
3 chr11:121592200-121592800 Enhancers Colon Smooth Muscle Colon
4 chr11:121592600-121592800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr11:121592600-121592800 Enhancers Cortex derived primary cultured neurospheres brain
6 chr11:121592600-121592800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr11:121592600-121592800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
8 chr11:121592600-121592800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr11:121592600-121592800 Enhancers Fetal Brain Male brain
10 chr11:121592600-121592800 Enhancers Rectal Smooth Muscle rectum
11 chr11:121592600-121592800 Enhancers Stomach Smooth Muscle stomach
12 chr11:121592600-121593000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
13 chr11:121592600-121593000 Enhancers HepG2 liver
14 chr11:121592600-121593200 Enhancers Primary hematopoietic stem cells blood
15 chr11:121592600-121593200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
16 chr11:121592600-121594000 Active TSS Fetal Brain Female brain
17 chr11:121592600-121594200 Active TSS Brain Germinal Matrix brain

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