Variant report

Variant rs9666628
Chromosome Location chr11:75938259-75938260
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:75935200-75940600 Enhancers Fetal Intestine Large intestine
2 chr11:75935200-75940600 Enhancers Fetal Intestine Small intestine
3 chr11:75936600-75938600 Weak transcription Fetal Muscle Leg muscle
4 chr11:75936600-75939200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr11:75936800-75939000 Weak transcription Fetal Muscle Trunk muscle
6 chr11:75936800-75939000 Enhancers HepG2 liver
7 chr11:75937000-75938800 Weak transcription Adipose Nuclei Adipose
8 chr11:75937000-75940400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr11:75937000-75945000 Weak transcription Right Atrium heart
10 chr11:75937000-75945000 Weak transcription Spleen Spleen
11 chr11:75937200-75939400 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr11:75937200-75941200 Weak transcription Skeletal Muscle Female skeletal muscle
13 chr11:75937400-75939800 Enhancers Primary monocytes fromperipheralblood blood
14 chr11:75937600-75940000 Enhancers Monocytes-CD14+_RO01746 blood
15 chr11:75937800-75940600 Weak transcription Placenta Amnion Placenta Amnion
16 chr11:75938200-75938600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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