Variant report

Variant rs7571007
Chromosome Location chr2:10961297-10961298
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:10953600-10968200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr2:10955400-10968600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr2:10960800-10961400 Enhancers Adipose Nuclei Adipose
4 chr2:10960800-10961400 Enhancers Gastric stomach
5 chr2:10960800-10961600 Enhancers Fetal Muscle Leg muscle
6 chr2:10960800-10961800 Enhancers Primary monocytes fromperipheralblood blood
7 chr2:10960800-10962000 Enhancers Monocytes-CD14+_RO01746 blood
8 chr2:10961000-10961400 Enhancers Brain Hippocampus Middle brain
9 chr2:10961000-10961600 Flanking Active TSS Stomach Mucosa stomach
10 chr2:10961200-10972400 Weak transcription Right Atrium heart

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