Variant report

Variant rs1778753
Chromosome Location chr1:145071235-145071236
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:145063400-145072400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:145067200-145071400 Weak transcription Muscle Satellite Cultured Cells --
3 chr1:145067200-145071600 Weak transcription Brain Anterior Caudate brain
4 chr1:145067600-145073800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:145068200-145074600 Weak transcription Osteobl bone
6 chr1:145070000-145074600 Weak transcription NHLF lung
7 chr1:145070200-145071600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr1:145070200-145073400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:145071000-145071400 Flanking Active TSS NHDF-Ad bronchial
10 chr1:145071200-145071400 Enhancers Brain Cingulate Gyrus brain
11 chr1:145071200-145071400 Active TSS Brain Inferior Temporal Lobe brain
12 chr1:145071200-145071400 Enhancers K562 blood
13 chr1:145071200-145071600 Flanking Active TSS Brain Angular Gyrus brain
14 chr1:145071200-145071600 Flanking Active TSS Brain Dorsolateral Prefrontal Cortex brain
15 chr1:145071200-145072400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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