Variant report

Variant rs1680639
Chromosome Location chr10:44701754-44701755
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44691600-44705200 Weak transcription Right Atrium heart
2 chr10:44698400-44701800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr10:44698800-44701800 Weak transcription HepG2 liver
4 chr10:44700200-44703000 Enhancers Fetal Muscle Leg muscle
5 chr10:44700400-44701800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr10:44700600-44701800 Enhancers Fetal Lung lung
7 chr10:44700600-44702400 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr10:44700800-44702000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr10:44700800-44702600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr10:44701000-44702200 Enhancers Fetal Stomach stomach
11 chr10:44701200-44701800 Enhancers Fetal Heart heart
12 chr10:44701200-44702000 Enhancers NHDF-Ad bronchial
13 chr10:44701200-44705000 Weak transcription iPS-18 Cell Line embryonic stem cell
14 chr10:44701200-44705400 Weak transcription HUES64 Cell Line embryonic stem cell
15 chr10:44701200-44705400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
16 chr10:44701600-44701800 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin01 Skin
17 chr10:44701600-44701800 Enhancers Ovary ovary
18 chr10:44701600-44703000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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