Variant report

Variant rs61779089
Chromosome Location chr1:92393041-92393042
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92386000-92393200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr1:92390200-92394800 Weak transcription Osteobl bone
3 chr1:92390600-92393800 Weak transcription NHDF-Ad bronchial
4 chr1:92391800-92393200 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr1:92391800-92393800 Weak transcription Fetal Heart heart
6 chr1:92391800-92394800 Weak transcription Fetal Muscle Leg muscle
7 chr1:92392000-92394600 Weak transcription NHLF lung
8 chr1:92392200-92394800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr1:92392600-92393200 Enhancers Hela-S3 cervix
10 chr1:92392800-92395800 Enhancers HepG2 liver
11 chr1:92393000-92393400 Enhancers Primary T helper memory cells from peripheral blood 2 blood
12 chr1:92393000-92393400 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr1:92393000-92393400 Enhancers Stomach Smooth Muscle stomach
14 chr1:92393000-92394000 Enhancers Fetal Kidney kidney
15 chr1:92393000-92394600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
16 chr1:92393000-92396000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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