Variant report

Variant rs11224343
Chromosome Location chr11:100511059-100511060
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:100501800-100512200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:100502000-100512800 Weak transcription Gastric stomach
3 chr11:100505000-100511200 Enhancers Placenta Placenta
4 chr11:100508200-100514400 Enhancers Fetal Lung lung
5 chr11:100508800-100511400 Weak transcription Fetal Muscle Leg muscle
6 chr11:100509400-100512000 Enhancers Fetal Heart heart
7 chr11:100509400-100513000 Enhancers Fetal Stomach stomach
8 chr11:100509600-100511600 Enhancers Stomach Mucosa stomach
9 chr11:100510000-100511800 Enhancers Brain Germinal Matrix brain
10 chr11:100510000-100513000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr11:100510400-100511200 Enhancers Brain Hippocampus Middle brain
12 chr11:100510800-100512800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr11:100511000-100511200 Enhancers Brain Cingulate Gyrus brain
14 chr11:100511000-100513200 Weak transcription Colon Smooth Muscle Colon
15 chr11:100511000-100518000 Weak transcription iPS-15b Cell Line embryonic stem cell

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