Variant report

Variant rs4764229
Chromosome Location chr12:10222905-10222906
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:10219000-10236800 Weak transcription Left Ventricle heart
2 chr12:10220000-10223000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
3 chr12:10220800-10234800 Weak transcription Placenta Placenta
4 chr12:10221200-10223400 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr12:10221400-10235000 Weak transcription Skeletal Muscle Male skeletal muscle
6 chr12:10222000-10223000 Enhancers Primary hematopoietic stem cells blood
7 chr12:10222000-10223400 Enhancers Primary B cells from cord blood blood
8 chr12:10222000-10223600 Enhancers Primary monocytes fromperipheralblood blood
9 chr12:10222000-10224200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr12:10222000-10224200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr12:10222000-10225400 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr12:10222000-10234800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr12:10222400-10227600 Weak transcription Adipose Nuclei Adipose
14 chr12:10222600-10223000 Flanking Active TSS Primary neutrophils fromperipheralblood blood
15 chr12:10222600-10224000 Enhancers GM12878-XiMat blood
16 chr12:10222800-10225200 Weak transcription HUVEC blood vessel
17 chr12:10222800-10248400 Weak transcription Psoas Muscle Psoas

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