Variant report

Variant rs553992046
Chromosome Location chr2:133281319-133281320
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133268200-133282800 Weak transcription Fetal Intestine Small intestine
2 chr2:133274400-133283200 Weak transcription Pancreas Pancrea
3 chr2:133279000-133282600 Enhancers Fetal Brain Male brain
4 chr2:133279200-133281600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:133279200-133283000 Weak transcription Fetal Heart heart
6 chr2:133280200-133281400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr2:133280200-133281400 Enhancers Fetal Brain Female brain
8 chr2:133281200-133281400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr2:133281200-133281800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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