Variant report

Variant rs538766572
Chromosome Location chr2:40613628-40613629
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:40601000-40621800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:40608400-40622000 Weak transcription Rectal Smooth Muscle rectum
3 chr2:40609600-40621800 Weak transcription Primary hematopoietic stem cells blood
4 chr2:40610000-40619000 Weak transcription Dnd41 blood
5 chr2:40611400-40616200 Weak transcription Left Ventricle heart
6 chr2:40612400-40613800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr2:40612600-40614000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr2:40612600-40614000 Weak transcription Osteobl bone
9 chr2:40612600-40622600 Weak transcription HSMM muscle
10 chr2:40612800-40613800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:40612800-40614000 Weak transcription Fetal Heart heart
12 chr2:40613000-40616000 Enhancers Monocytes-CD14+_RO01746 blood
13 chr2:40613000-40618800 Weak transcription Colon Smooth Muscle Colon
14 chr2:40613000-40619200 Weak transcription Primary neutrophils fromperipheralblood blood
15 chr2:40613600-40617200 Weak transcription Primary monocytes fromperipheralblood blood

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