Variant report

Variant rs564651312
Chromosome Location chr7:11210453-11210454
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr7:11193200-11211200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr7:11204200-11213200 Weak transcription Primary B cells from cord blood blood
9 chr7:11204400-11217400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr7:11207000-11226000 Weak transcription Gastric stomach
11 chr7:11209000-11211400 Weak transcription HUVEC blood vessel
12 chr7:11209600-11210600 Enhancers Liver Liver
13 chr7:11209600-11210800 Enhancers Fetal Brain Male brain
14 chr7:11210000-11211000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr7:11210000-11211000 Enhancers Adipose Nuclei Adipose
16 chr7:11210000-11211000 Enhancers Monocytes-CD14+_RO01746 blood
17 chr7:11210000-11211600 Enhancers Fetal Brain Female brain
18 chr7:11210200-11210600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
19 chr7:11210200-11211800 Enhancers Fetal Lung lung

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