Variant report

Variant rs5019164
Chromosome Location chr11:67438492-67438493
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr11:67437200-67441600 Weak transcription Gastric stomach
5 chr11:67437800-67439000 Genic enhancers Esophagus oesophagus
6 chr11:67438000-67438600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr11:67438000-67439000 Enhancers Dnd41 blood
8 chr11:67438000-67442000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr11:67438200-67438600 Enhancers Primary hematopoietic stem cells blood
10 chr11:67438400-67438800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr11:67438400-67438800 Enhancers Primary B cells from cord blood blood
12 chr11:67438400-67439000 Enhancers Fetal Thymus thymus

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