Variant report

Variant rs12132227
Chromosome Location chr1:246294482-246294483
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246271200-246302200 Weak transcription Osteobl bone
2 chr1:246272400-246312000 Weak transcription Gastric stomach
3 chr1:246274000-246301400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:246277400-246297200 Weak transcription Aorta Aorta
5 chr1:246277800-246327800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr1:246281000-246304000 Weak transcription Primary T cells from cord blood blood
7 chr1:246281200-246310800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr1:246281200-246311400 Weak transcription Primary B cells from cord blood blood
9 chr1:246281200-246311400 Weak transcription Primary hematopoietic stem cells blood
10 chr1:246281800-246306400 Weak transcription Primary T helper cells fromperipheralblood blood
11 chr1:246285800-246302200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:246294000-246295000 Enhancers HUVEC blood vessel
13 chr1:246294200-246294600 Enhancers Stomach Mucosa stomach
14 chr1:246294200-246294800 Enhancers K562 blood

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