Variant report

Variant rs4654179
Chromosome Location chr1:246144436-246144437
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246121000-246166200 Weak transcription Primary T cells from cord blood blood
2 chr1:246133000-246149800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:246141200-246144600 Strong transcription K562 blood
4 chr1:246142000-246145800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr1:246142000-246152600 Weak transcription Esophagus oesophagus
6 chr1:246142400-246144600 Weak transcription Primary B cells from cord blood blood
7 chr1:246142800-246149000 Weak transcription Osteobl bone
8 chr1:246142800-246149800 Weak transcription HSMMtube muscle
9 chr1:246143400-246144600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr1:246143600-246149800 Weak transcription Aorta Aorta
11 chr1:246143800-246145200 Weak transcription Placenta Amnion Placenta Amnion
12 chr1:246143800-246151000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr1:246144200-246144600 Enhancers Fetal Stomach stomach
14 chr1:246144200-246154200 Weak transcription Placenta Placenta
15 chr1:246144400-246149800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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