Variant report

Variant rs415179
Chromosome Location chr6:29885606-29885607
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29868600-29893800 Weak transcription Aorta Aorta
2 chr6:29876400-29893800 Weak transcription Gastric stomach
3 chr6:29878600-29892400 Weak transcription Duodenum Mucosa Duodenum
4 chr6:29878600-29892600 Weak transcription Esophagus oesophagus
5 chr6:29879200-29885800 Weak transcription Fetal Intestine Large intestine
6 chr6:29879200-29886200 Weak transcription Fetal Intestine Small intestine
7 chr6:29883000-29892600 Weak transcription Stomach Mucosa stomach
8 chr6:29883400-29886800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr6:29884200-29888600 Enhancers Primary monocytes fromperipheralblood blood
10 chr6:29884600-29888600 Enhancers Primary neutrophils fromperipheralblood blood
11 chr6:29885400-29886000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr6:29885600-29885800 Enhancers Spleen Spleen

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