Variant report

Variant rs1891743
Chromosome Location chr1:224270258-224270259
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:224268000-224270600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr1:224268600-224270400 Enhancers K562 blood
3 chr1:224268600-224275000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr1:224269200-224270600 Enhancers NH-A brain
5 chr1:224269600-224270400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr1:224269600-224270400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr1:224269600-224270800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr1:224269800-224270400 Enhancers H9 Cell Line embryonic stem cell
9 chr1:224269800-224270400 Enhancers HUES6 Cell Line embryonic stem cell
10 chr1:224269800-224270400 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr1:224269800-224270600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:224270200-224270400 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
13 chr1:224270200-224275000 Weak transcription HUVEC blood vessel

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