Variant report

Variant rs1778761
Chromosome Location chr1:145066917-145066918
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145061000-145068200 Weak transcription Brain Angular Gyrus brain
2 chr1:145061000-145071200 Weak transcription Brain Inferior Temporal Lobe brain
3 chr1:145062800-145068400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr1:145062800-145069000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr1:145063400-145072400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr1:145065600-145067000 ZNF genes & repeats Osteobl bone
7 chr1:145065600-145068600 ZNF genes & repeats NHDF-Ad bronchial
8 chr1:145065800-145067000 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:145065800-145067200 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:145065800-145067200 ZNF genes & repeats Muscle Satellite Cultured Cells --
11 chr1:145066000-145067600 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr1:145066200-145067600 ZNF genes & repeats Primary T cells from cord blood blood
13 chr1:145066800-145067800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain

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