Variant report

Variant rs532636415
Chromosome Location chr5:16655631-16655632
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:16650000-16664600 Weak transcription H1 Cell Line embryonic stem cell
2 chr5:16652600-16663000 Weak transcription Primary T cells from cord blood blood
3 chr5:16653800-16663600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr5:16655600-16655800 Enhancers Esophagus oesophagus
5 chr5:16655600-16655800 ZNF genes & repeats Pancreas Pancrea
6 chr5:16655600-16655800 Bivalent Enhancer NHDF-Ad bronchial

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