Variant report

Variant rs34174478
Chromosome Location chr1:92393291-92393292
allele -/A
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92390200-92394800 Weak transcription Osteobl bone
2 chr1:92390600-92393800 Weak transcription NHDF-Ad bronchial
3 chr1:92391800-92393800 Weak transcription Fetal Heart heart
4 chr1:92391800-92394800 Weak transcription Fetal Muscle Leg muscle
5 chr1:92392000-92394600 Weak transcription NHLF lung
6 chr1:92392200-92394800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr1:92392800-92395800 Enhancers HepG2 liver
8 chr1:92393000-92393400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
9 chr1:92393000-92393400 Enhancers Primary Natural Killer cells fromperipheralblood blood
10 chr1:92393000-92393400 Enhancers Stomach Smooth Muscle stomach
11 chr1:92393000-92394000 Enhancers Fetal Kidney kidney
12 chr1:92393000-92394600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr1:92393000-92396000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:92393200-92394000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr1:92393200-92394000 Enhancers Fetal Stomach stomach
16 chr1:92393200-92394600 Weak transcription Hela-S3 cervix
17 chr1:92393200-92395800 Enhancers Fetal Adrenal Gland Adrenal Gland

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