Variant report

Variant rs10247599
Chromosome Location chr7:11211307-11211308
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:11107600-11212200 Weak transcription Fetal Kidney kidney
2 chr7:11113200-11211800 Weak transcription Fetal Intestine Large intestine
3 chr7:11170600-11217400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr7:11175400-11213200 Weak transcription Primary Natural Killer cells fromperipheralblood blood
5 chr7:11189200-11214000 Weak transcription Primary hematopoietic stem cells blood
6 chr7:11190000-11213200 Weak transcription Dnd41 blood
7 chr7:11204200-11213200 Weak transcription Primary B cells from cord blood blood
8 chr7:11204400-11217400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr7:11207000-11226000 Weak transcription Gastric stomach
10 chr7:11209000-11211400 Weak transcription HUVEC blood vessel
11 chr7:11210000-11211600 Enhancers Fetal Brain Female brain
12 chr7:11210200-11211800 Enhancers Fetal Lung lung
13 chr7:11210600-11211400 Enhancers Pancreatic Islets Pancreatic Islet
14 chr7:11211000-11212200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr7:11211200-11211600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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