Variant report

Variant rs9907962
Chromosome Location chr17:60188912-60188913
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:60184200-60189200 Weak transcription K562 blood
2 chr17:60186600-60189200 Enhancers HepG2 liver
3 chr17:60186800-60189800 Enhancers A549 lung
4 chr17:60187000-60189000 Weak transcription GM12878-XiMat blood
5 chr17:60187000-60189800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr17:60187400-60189600 Enhancers Duodenum Mucosa Duodenum
7 chr17:60188000-60189400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr17:60188200-60189600 Enhancers Fetal Intestine Small intestine
9 chr17:60188400-60189400 Enhancers Muscle Satellite Cultured Cells --
10 chr17:60188400-60189600 Enhancers Stomach Mucosa stomach
11 chr17:60188400-60189800 Enhancers Fetal Intestine Large intestine
12 chr17:60188600-60189400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
13 chr17:60188600-60189400 Enhancers Placenta Placenta
14 chr17:60188600-60189600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr17:60188800-60189400 Flanking Active TSS Rectal Mucosa Donor 29 rectum
16 chr17:60188800-60189600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr17:60188800-60189600 Flanking Active TSS Rectal Mucosa Donor 31 rectum

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