Variant report

Variant rs1551887
Chromosome Location chr11:67433758-67433759
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67427000-67433800 Weak transcription Dnd41 blood
2 chr11:67430600-67440800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr11:67430800-67435200 Weak transcription Primary hematopoietic stem cells blood
4 chr11:67431200-67437800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr11:67433000-67434000 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr11:67433000-67434400 Genic enhancers Placenta Placenta
7 chr11:67433200-67434000 Enhancers Fetal Intestine Small intestine
8 chr11:67433200-67435400 Enhancers Fetal Thymus thymus
9 chr11:67433400-67436600 Enhancers Primary B cells from peripheral blood blood
10 chr11:67433600-67433800 Enhancers Esophagus oesophagus
11 chr11:67433600-67435400 Enhancers Primary B cells from cord blood blood

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