Variant report

Variant rs534656903
Chromosome Location chr13:39526050-39526051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:39520200-39541600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr13:39521800-39526200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr13:39525400-39526400 Enhancers Rectal Mucosa Donor 31 rectum
4 chr13:39525400-39526800 Weak transcription Pancreas Pancrea
5 chr13:39525800-39526400 Enhancers Cortex derived primary cultured neurospheres brain
6 chr13:39525800-39526400 Active TSS Pancreatic Islets Pancreatic Islet
7 chr13:39525800-39526400 Active TSS Rectal Mucosa Donor 29 rectum
8 chr13:39525800-39526400 Flanking Active TSS HUVEC blood vessel
9 chr13:39525800-39526600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr13:39526000-39526200 Active TSS Ganglion Eminence derived primary cultured neurospheres brain
11 chr13:39526000-39526200 Active TSS Adipose Nuclei Adipose
12 chr13:39526000-39526200 Active TSS Duodenum Mucosa Duodenum
13 chr13:39526000-39526400 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr13:39526000-39526400 Active TSS Right Atrium heart

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