Variant report

Variant rs35059012
Chromosome Location chr2:33317367-33317368
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33309000-33333600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr2:33309200-33329000 Weak transcription K562 blood
3 chr2:33311400-33327800 Weak transcription Fetal Kidney kidney
4 chr2:33311800-33328000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr2:33312600-33329400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:33312800-33325600 Weak transcription Fetal Lung lung
7 chr2:33315200-33318200 Enhancers Fetal Heart heart
8 chr2:33316000-33317400 Enhancers Fetal Adrenal Gland Adrenal Gland
9 chr2:33316000-33318000 Enhancers Aorta Aorta
10 chr2:33316000-33319800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:33316200-33317600 Enhancers Ovary ovary
12 chr2:33316800-33318000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
13 chr2:33317000-33318000 Enhancers Stomach Smooth Muscle stomach
14 chr2:33317000-33318200 Enhancers Right Atrium heart
15 chr2:33317200-33317400 Enhancers Skeletal Muscle Female skeletal muscle
16 chr2:33317200-33318000 Enhancers Left Ventricle heart
17 chr2:33317200-33318400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
18 chr2:33317200-33318600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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