Variant report

Variant rs12672248
Chromosome Location chr7:3559904-3559905
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:3549400-3577000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:3554800-3563000 Weak transcription Aorta Aorta
3 chr7:3557400-3560600 Weak transcription Pancreas Pancrea
4 chr7:3557600-3562800 Weak transcription Primary neutrophils fromperipheralblood blood
5 chr7:3559000-3560000 Weak transcription Colon Smooth Muscle Colon
6 chr7:3559600-3560200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr7:3559600-3560400 Enhancers HepG2 liver
8 chr7:3559600-3560600 Enhancers Primary T cells from cord blood blood
9 chr7:3559600-3560800 Enhancers Fetal Heart heart
10 chr7:3559600-3560800 Enhancers Fetal Intestine Large intestine
11 chr7:3559800-3560200 Active TSS Pancreatic Islets Pancreatic Islet
12 chr7:3559800-3560200 Enhancers Fetal Lung lung
13 chr7:3559800-3560800 Enhancers Primary T helper naive cells fromperipheralblood blood

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