Variant report

Variant rs7488727
Chromosome Location chr12:38780061-38780062
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:38778400-38780600 Enhancers HUES64 Cell Line embryonic stem cell
2 chr12:38778800-38780200 Active TSS ES-WA7 Cell Line embryonic stem cell
3 chr12:38779200-38780200 Enhancers Primary monocytes fromperipheralblood blood
4 chr12:38779600-38780200 Enhancers HUES6 Cell Line embryonic stem cell
5 chr12:38779600-38780600 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr12:38779600-38780600 Weak transcription iPS-18 Cell Line embryonic stem cell
7 chr12:38779600-38780600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr12:38779600-38784600 Weak transcription HMEC breast
9 chr12:38779800-38783600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr12:38780000-38780200 Flanking Active TSS A549 lung
11 chr12:38780000-38780400 Enhancers Hela-S3 cervix
12 chr12:38780000-38780400 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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