Variant report

Variant rs7767708
Chromosome Location chr6:167289905-167289906
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167281400-167291200 Weak transcription Primary B cells from peripheral blood blood
2 chr6:167287000-167290600 Weak transcription Placenta Amnion Placenta Amnion
3 chr6:167288000-167290000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr6:167288000-167290000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr6:167288000-167291600 Weak transcription Gastric stomach
6 chr6:167289800-167290000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr6:167289800-167291400 Strong transcription Primary B cells from cord blood blood

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