Variant report

Variant rs16896982
Chromosome Location chr4:18404137-18404138
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:18391600-18404800 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr4:18400600-18404400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr4:18401400-18408800 Enhancers Fetal Intestine Large intestine
4 chr4:18401400-18409200 Enhancers Fetal Intestine Small intestine
5 chr4:18402800-18405000 Enhancers Duodenum Mucosa Duodenum
6 chr4:18403800-18406400 Weak transcription Small Intestine intestine
7 chr4:18403800-18411800 Weak transcription Breast Myoepithelial Primary Cells Breast

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