Variant report

Variant rs1611218
Chromosome Location chr6:29761717-29761718
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29760400-29764400 Weak transcription Hela-S3 cervix
2 chr6:29761000-29761800 Enhancers Pancreas Pancrea
3 chr6:29761000-29762000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
4 chr6:29761000-29763000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
5 chr6:29761000-29765200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr6:29761200-29762200 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr6:29761200-29763800 Weak transcription HMEC breast
8 chr6:29761200-29763800 Weak transcription NHEK skin
9 chr6:29761200-29764400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr6:29761400-29763800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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