Variant report

Variant rs11752672
Chromosome Location chr6:31896874-31896875
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:31895600-31897200 Enhancers Spleen Spleen
2 chr6:31895800-31901200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr6:31896000-31897200 Flanking Active TSS HepG2 liver
4 chr6:31896000-31898600 Enhancers Monocytes-CD14+_RO01746 blood
5 chr6:31896000-31901000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:31896000-31903400 Weak transcription Fetal Intestine Small intestine
7 chr6:31896200-31898600 Enhancers Placenta Placenta
8 chr6:31896400-31897200 Flanking Active TSS Liver Liver
9 chr6:31896400-31897200 Enhancers Small Intestine intestine
10 chr6:31896600-31897200 Enhancers Adipose Nuclei Adipose
11 chr6:31896800-31897200 Enhancers Duodenum Mucosa Duodenum
12 chr6:31896800-31897800 Enhancers Primary monocytes fromperipheralblood blood
13 chr6:31896800-31913000 Weak transcription Lung lung

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