Variant report

Variant rs2368560
Chromosome Location chr14:104273311-104273312
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104218400-104277800 Weak transcription Spleen Spleen
2 chr14:104241000-104274400 Weak transcription Colon Smooth Muscle Colon
3 chr14:104257800-104284000 Weak transcription Gastric stomach
4 chr14:104258800-104274800 Weak transcription Primary T cells fromperipheralblood blood
5 chr14:104262600-104277200 Weak transcription Pancreas Pancrea
6 chr14:104263000-104277400 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr14:104263200-104281800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr14:104263600-104274600 Weak transcription Liver Liver
9 chr14:104263800-104275800 Weak transcription Fetal Adrenal Gland Adrenal Gland
10 chr14:104268600-104285600 Weak transcription Lung lung
11 chr14:104270200-104273800 Enhancers Fetal Heart heart
12 chr14:104271000-104285600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr14:104272000-104273800 Flanking Active TSS GM12878-XiMat blood
14 chr14:104272200-104273600 Enhancers Stomach Mucosa stomach
15 chr14:104272600-104274000 Enhancers Left Ventricle heart
16 chr14:104272800-104273600 Enhancers Primary mononuclear cells fromperipheralblood Blood
17 chr14:104272800-104273600 Enhancers Right Ventricle heart
18 chr14:104273000-104273400 Enhancers Primary B cells from peripheral blood blood
19 chr14:104273200-104273400 Enhancers Primary T helper naive cells from peripheral blood blood
20 chr14:104273200-104273400 Enhancers Brain Angular Gyrus brain

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