Variant report

Variant rs2508339
Chromosome Location chr11:59477011-59477012
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59472400-59478200 Enhancers NHEK skin
2 chr11:59472800-59478200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr11:59472800-59478200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr11:59473800-59478200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr11:59475000-59477800 Weak transcription Hela-S3 cervix
6 chr11:59475400-59483200 Weak transcription K562 blood
7 chr11:59476400-59477200 Enhancers NHLF lung
8 chr11:59476400-59477800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr11:59476400-59477800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr11:59476400-59477800 Weak transcription A549 lung
11 chr11:59476400-59478000 Weak transcription HMEC breast
12 chr11:59476600-59478000 Weak transcription HSMM muscle
13 chr11:59476800-59477200 Weak transcription Muscle Satellite Cultured Cells --
14 chr11:59476800-59477200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr11:59476800-59477800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr11:59476800-59478000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr11:59477000-59477200 Enhancers Osteobl bone
18 chr11:59477000-59478200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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