Variant report

Variant rs7773215
Chromosome Location chr6:12492656-12492657
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:12489600-12493000 Enhancers NHDF-Ad bronchial
2 chr6:12490000-12493000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr6:12490200-12493200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr6:12490200-12493600 Enhancers Hela-S3 cervix
5 chr6:12490400-12493000 Enhancers Muscle Satellite Cultured Cells --
6 chr6:12491200-12493200 Enhancers HUVEC blood vessel
7 chr6:12491800-12493000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr6:12491800-12493000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
9 chr6:12491800-12494600 Weak transcription Pancreas Pancrea
10 chr6:12492000-12493200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr6:12492000-12494200 Weak transcription Spleen Spleen
12 chr6:12492000-12506000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr6:12492200-12493000 Weak transcription A549 lung
14 chr6:12492400-12494000 Weak transcription Placenta Placenta
15 chr6:12492600-12493800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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