Variant report

Variant rs188379148
Chromosome Location chr2:40612623-40612624
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr2:40611000-40612800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr2:40611000-40613600 Enhancers Primary monocytes fromperipheralblood blood
7 chr2:40611200-40612800 Enhancers Fetal Heart heart
8 chr2:40611200-40613000 Enhancers Primary neutrophils fromperipheralblood blood
9 chr2:40611400-40613000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
10 chr2:40611400-40616200 Weak transcription Left Ventricle heart
11 chr2:40612200-40612800 Enhancers HSMMtube muscle
12 chr2:40612400-40612800 Enhancers Duodenum Smooth Muscle Duodenum
13 chr2:40612400-40613000 Enhancers Colon Smooth Muscle Colon
14 chr2:40612400-40613800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
15 chr2:40612600-40614000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr2:40612600-40614000 Weak transcription Osteobl bone
17 chr2:40612600-40622600 Weak transcription HSMM muscle

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