Variant report

Variant rs553595190
Chromosome Location chr11:67512807-67512808
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67499800-67515200 Weak transcription Right Atrium heart
2 chr11:67500000-67521400 Weak transcription Placenta Amnion Placenta Amnion
3 chr11:67511000-67513000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr11:67511200-67513000 Enhancers Fetal Heart heart
5 chr11:67512400-67521000 Weak transcription Placenta Placenta
6 chr11:67512600-67513000 Flanking Active TSS Fetal Lung lung
7 chr11:67512600-67513000 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
8 chr11:67512600-67513200 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:67512600-67513200 Enhancers Esophagus oesophagus
10 chr11:67512600-67513200 ZNF genes & repeats Fetal Kidney kidney
11 chr11:67512600-67513200 ZNF genes & repeats Gastric stomach
12 chr11:67512600-67513200 Active TSS Pancreas Pancrea
13 chr11:67512600-67513200 Enhancers Spleen Spleen
14 chr11:67512800-67513000 Flanking Active TSS H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr11:67512800-67513200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr11:67512800-67513200 Genic enhancers iPS DF 6.9 Cell Line embryonic stem cell
17 chr11:67512800-67513200 Bivalent/Poised TSS NHDF-Ad bronchial

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