Variant report

Variant rs7486553
Chromosome Location chr12:38779006-38779007
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:38778000-38779800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr12:38778400-38780600 Enhancers HUES64 Cell Line embryonic stem cell
3 chr12:38778600-38779200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr12:38778800-38779200 Active TSS iPS-20b Cell Line embryonic stem cell
5 chr12:38778800-38779400 Active TSS iPS-18 Cell Line embryonic stem cell
6 chr12:38778800-38779400 Enhancers Placenta Placenta
7 chr12:38778800-38779400 Active TSS HepG2 liver
8 chr12:38778800-38779600 Active TSS ES-I3 Cell Line embryonic stem cell
9 chr12:38778800-38779600 Flanking Active TSS HUES6 Cell Line embryonic stem cell
10 chr12:38778800-38779600 Flanking Active TSS iPS-15b Cell Line embryonic stem cell
11 chr12:38778800-38780200 Active TSS ES-WA7 Cell Line embryonic stem cell
12 chr12:38779000-38779400 Flanking Active TSS HUES48 Cell Line embryonic stem cell
13 chr12:38779000-38779600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr12:38779000-38779600 Enhancers HMEC breast
15 chr12:38779000-38780000 Active TSS A549 lung
16 chr12:38779000-38780000 Flanking Active TSS Hela-S3 cervix

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