Variant report

Variant rs41291526
Chromosome Location chr1:77095084-77095085
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77088200-77098000 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr1:77090000-77099000 Weak transcription Brain Angular Gyrus brain
3 chr1:77093000-77097000 Weak transcription Left Ventricle heart
4 chr1:77093800-77095200 Strong transcription Primary B cells from cord blood blood
5 chr1:77093800-77096000 Weak transcription Brain Substantia Nigra brain
6 chr1:77094400-77095400 Strong transcription Fetal Lung lung
7 chr1:77094400-77098400 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr1:77094600-77095200 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr1:77094800-77098400 Weak transcription Brain Cingulate Gyrus brain
10 chr1:77095000-77097600 Weak transcription Fetal Intestine Large intestine
11 chr1:77095000-77098200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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