Variant report

Variant rs4557563
Chromosome Location chr6:110215527-110215528
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:110210600-110215600 Enhancers Placenta Placenta
2 chr6:110211800-110218400 Enhancers Primary monocytes fromperipheralblood blood
3 chr6:110212400-110216800 Flanking Active TSS Monocytes-CD14+_RO01746 blood
4 chr6:110212800-110215600 Enhancers Primary Natural Killer cells fromperipheralblood blood
5 chr6:110212800-110218800 Enhancers Primary B cells from peripheral blood blood
6 chr6:110213000-110216400 Flanking Active TSS Primary neutrophils fromperipheralblood blood
7 chr6:110214400-110215600 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
8 chr6:110214800-110215600 ZNF genes & repeats H9 Cell Line embryonic stem cell
9 chr6:110214800-110215600 Enhancers Esophagus oesophagus
10 chr6:110214800-110215800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr6:110214800-110215800 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
12 chr6:110214800-110216800 ZNF genes & repeats H1 Cell Line embryonic stem cell
13 chr6:110214800-110216800 ZNF genes & repeats HUES48 Cell Line embryonic stem cell
14 chr6:110215000-110215600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
15 chr6:110215000-110215600 ZNF genes & repeats Primary hematopoietic stem cells blood
16 chr6:110215200-110218800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr6:110215400-110215600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
18 chr6:110215400-110216400 Flanking Active TSS Primary B cells from cord blood blood
19 chr6:110215400-110217600 Weak transcription Brain Hippocampus Middle brain
20 chr6:110215400-110217800 Weak transcription Stomach Mucosa stomach

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