Variant report

Variant rs11165818
Chromosome Location chr1:92393986-92393987
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:92390200-92394800 Weak transcription Osteobl bone
2 chr1:92391800-92394800 Weak transcription Fetal Muscle Leg muscle
3 chr1:92392000-92394600 Weak transcription NHLF lung
4 chr1:92392200-92394800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr1:92392800-92395800 Enhancers HepG2 liver
6 chr1:92393000-92394000 Enhancers Fetal Kidney kidney
7 chr1:92393000-92394600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr1:92393000-92396000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr1:92393200-92394000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr1:92393200-92394000 Enhancers Fetal Stomach stomach
11 chr1:92393200-92394600 Weak transcription Hela-S3 cervix
12 chr1:92393200-92395800 Enhancers Fetal Adrenal Gland Adrenal Gland
13 chr1:92393400-92394400 Weak transcription Stomach Smooth Muscle stomach
14 chr1:92393800-92394000 Enhancers Fetal Heart heart
15 chr1:92393800-92394200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
16 chr1:92393800-92394400 Enhancers Ovary ovary
17 chr1:92393800-92394800 Weak transcription Fetal Lung lung
18 chr1:92393800-92395800 Enhancers NHDF-Ad bronchial

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