Variant report

Variant rs34790329
Chromosome Location chr12:38779941-38779942
allele C/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 chr12:38779000-38780000 Active TSS A549 lung
4 chr12:38779000-38780000 Flanking Active TSS Hela-S3 cervix
5 chr12:38779200-38780200 Enhancers Primary monocytes fromperipheralblood blood
6 chr12:38779600-38780000 Enhancers Monocytes-CD14+_RO01746 blood
7 chr12:38779600-38780200 Enhancers HUES6 Cell Line embryonic stem cell
8 chr12:38779600-38780600 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr12:38779600-38780600 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr12:38779600-38780600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
11 chr12:38779600-38784600 Weak transcription HMEC breast
12 chr12:38779800-38783600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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