Variant report

Variant rs4081311
Chromosome Location chr1:246672337-246672338
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246671200-246675000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr1:246671200-246676000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr1:246672200-246672400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:246672200-246672400 Enhancers Esophagus oesophagus
5 chr1:246672200-246672400 Enhancers Fetal Stomach stomach
6 chr1:246672200-246672400 Enhancers Stomach Smooth Muscle stomach
7 chr1:246672200-246672400 Flanking Active TSS HepG2 liver
8 chr1:246672200-246672600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell

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