Variant report

Variant rs28592003
Chromosome Location chr7:17167540-17167541
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17162800-17170600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
2 chr7:17163000-17170200 Weak transcription Aorta Aorta
3 chr7:17163400-17169800 Weak transcription Muscle Satellite Cultured Cells --
4 chr7:17163400-17169800 Weak transcription NHLF lung
5 chr7:17166000-17168000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr7:17166200-17170000 Weak transcription Brain Substantia Nigra brain
7 chr7:17166600-17167800 Enhancers Monocytes-CD14+_RO01746 blood
8 chr7:17166800-17167800 Enhancers Primary monocytes fromperipheralblood blood
9 chr7:17167000-17169600 Weak transcription Fetal Intestine Small intestine
10 chr7:17167200-17169400 Weak transcription Fetal Intestine Large intestine
11 chr7:17167400-17167600 Enhancers GM12878-XiMat blood
12 chr7:17167400-17168600 Weak transcription HepG2 liver

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