Variant report

Variant rs9259713
Chromosome Location chr6:29883036-29883037
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 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 chr6:29877400-29885600 Weak transcription Spleen Spleen
4 chr6:29878600-29892400 Weak transcription Duodenum Mucosa Duodenum
5 chr6:29878600-29892600 Weak transcription Esophagus oesophagus
6 chr6:29879200-29885800 Weak transcription Fetal Intestine Large intestine
7 chr6:29879200-29886200 Weak transcription Fetal Intestine Small intestine
8 chr6:29881600-29883400 Weak transcription HepG2 liver
9 chr6:29882200-29883400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr6:29883000-29883200 Enhancers Placenta Amnion Placenta Amnion
11 chr6:29883000-29892600 Weak transcription Stomach Mucosa stomach

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