Variant report

Variant rs3998676
Chromosome Location chr6:29887564-29887565
allele C/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 chr6:29883000-29892600 Weak transcription Stomach Mucosa stomach
6 chr6:29884200-29888600 Enhancers Primary monocytes fromperipheralblood blood
7 chr6:29884600-29888600 Enhancers Primary neutrophils fromperipheralblood blood
8 chr6:29885800-29893800 Weak transcription Spleen Spleen
9 chr6:29886000-29887600 Enhancers Monocytes-CD14+_RO01746 blood
10 chr6:29886600-29892600 Weak transcription Fetal Intestine Large intestine
11 chr6:29886800-29888800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr6:29887000-29892000 Weak transcription Fetal Intestine Small intestine

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