Variant report

Variant rs9857242
Chromosome Location chr3:134316378-134316379
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:134311600-134320400 Flanking Active TSS Primary neutrophils fromperipheralblood blood
2 chr3:134313400-134319400 Weak transcription Skeletal Muscle Female skeletal muscle
3 chr3:134313400-134321600 Weak transcription Spleen Spleen
4 chr3:134313600-134316600 Weak transcription Primary B cells from cord blood blood
5 chr3:134314600-134316400 Weak transcription Primary hematopoietic stem cells blood
6 chr3:134315600-134317000 Enhancers Esophagus oesophagus
7 chr3:134315600-134317800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr3:134315800-134316800 Enhancers Pancreas Pancrea
9 chr3:134315800-134317200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr3:134315800-134317800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr3:134315800-134317800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr3:134315800-134318400 Enhancers Primary monocytes fromperipheralblood blood
13 chr3:134316000-134317200 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr3:134316200-134316400 Flanking Active TSS NHEK skin
15 chr3:134316200-134317400 Enhancers Monocytes-CD14+_RO01746 blood
16 chr3:134316200-134317600 Enhancers HMEC breast

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