Variant report

Variant rs56141916
Chromosome Location chr6:27259544-27259545
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:27257800-27259600 Bivalent/Poised TSS HUES48 Cell Line embryonic stem cell
2 chr6:27257800-27260000 Active TSS H9 Cell Line embryonic stem cell
3 chr6:27258000-27259600 Bivalent/Poised TSS iPS-20b Cell Line embryonic stem cell
4 chr6:27258000-27260000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
5 chr6:27258000-27261800 ZNF genes & repeats Pancreatic Islets Pancreatic Islet
6 chr6:27258400-27261200 Weak transcription HMEC breast
7 chr6:27258800-27261000 Weak transcription A549 lung
8 chr6:27259200-27260000 Enhancers K562 blood
9 chr6:27259200-27261200 Weak transcription NHEK skin
10 chr6:27259400-27259600 Bivalent/Poised TSS HUES6 Cell Line embryonic stem cell
11 chr6:27259400-27259600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
12 chr6:27259400-27261000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:27259400-27261200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr6:27259400-27263400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr6:27259400-27263600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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