Variant report

Variant rs60769229
Chromosome Location chr1:173496078-173496079
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173488400-173496800 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr1:173491000-173496400 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr1:173494800-173497000 Enhancers Adipose Nuclei Adipose
4 chr1:173494800-173497800 Enhancers Hela-S3 cervix
5 chr1:173495000-173500200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr1:173495200-173496800 Enhancers Fetal Adrenal Gland Adrenal Gland
7 chr1:173495400-173496400 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr1:173495400-173496400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr1:173495400-173497000 Enhancers Liver Liver
10 chr1:173495600-173496800 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:173495600-173497200 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr1:173495800-173496800 Enhancers Placenta Placenta
13 chr1:173496000-173496800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:173496000-173496800 Enhancers HMEC breast
15 chr1:173496000-173497400 Enhancers Right Atrium heart

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