Variant report

Variant rs555110841
Chromosome Location chr11:67437972-67437973
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67430600-67440800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr11:67434000-67442400 Weak transcription Fetal Intestine Small intestine
3 chr11:67434400-67438600 Enhancers Placenta Placenta
4 chr11:67435600-67438200 Weak transcription Primary hematopoietic stem cells blood
5 chr11:67435600-67438400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr11:67437000-67438400 Weak transcription Primary B cells from cord blood blood
7 chr11:67437200-67441600 Weak transcription Gastric stomach
8 chr11:67437800-67438000 Flanking Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr11:67437800-67438000 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr11:67437800-67438000 Enhancers Fetal Thymus thymus
11 chr11:67437800-67438000 Flanking Active TSS Dnd41 blood
12 chr11:67437800-67438400 Enhancers Thymus Thymus
13 chr11:67437800-67439000 Genic enhancers Esophagus oesophagus

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