Variant report

Variant rs11578772
Chromosome Location chr1:145561116-145561117
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145549800-145561800 Weak transcription Right Atrium heart
2 chr1:145550200-145562200 Weak transcription Right Ventricle heart
3 chr1:145550200-145562400 Weak transcription Brain Angular Gyrus brain
4 chr1:145550400-145562400 Weak transcription Brain Hippocampus Middle brain
5 chr1:145550800-145562000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr1:145551400-145561800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:145555400-145561800 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr1:145555600-145562600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr1:145557000-145562200 Weak transcription HMEC breast
10 chr1:145557000-145562600 Weak transcription Gastric stomach
11 chr1:145558600-145562400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr1:145558600-145562400 Weak transcription Pancreas Pancrea
13 chr1:145559000-145561600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr1:145559200-145562200 Weak transcription Esophagus oesophagus
15 chr1:145560200-145561600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr1:145560600-145562400 Enhancers Placenta Amnion Placenta Amnion
17 chr1:145561000-145561400 Genic enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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