Variant report

Variant rs10924419
Chromosome Location chr1:246142620-246142621
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr1:246131200-246143200 Weak transcription Aorta Aorta
3 chr1:246132400-246142800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:246133000-246149800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:246141200-246144600 Strong transcription K562 blood
6 chr1:246141400-246143400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr1:246142000-246142800 Enhancers HSMMtube muscle
8 chr1:246142000-246142800 Enhancers Osteobl bone
9 chr1:246142000-246143800 Enhancers Placenta Amnion Placenta Amnion
10 chr1:246142000-246145800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr1:246142000-246152600 Weak transcription Esophagus oesophagus
12 chr1:246142200-246142800 Enhancers Muscle Satellite Cultured Cells --
13 chr1:246142200-246142800 Enhancers NH-A brain
14 chr1:246142200-246143000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr1:246142200-246144400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr1:246142400-246144600 Weak transcription Primary B cells from cord blood blood

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