Variant report

Variant rs2970056
Chromosome Location chr17:50220886-50220887
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:50216000-50221200 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr17:50216200-50222600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr17:50216400-50222000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr17:50219200-50221000 Weak transcription H1 Cell Line embryonic stem cell
5 chr17:50219200-50222400 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr17:50219200-50223000 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr17:50219600-50221000 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr17:50219600-50221000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr17:50219600-50222400 Weak transcription iPS-20b Cell Line embryonic stem cell
10 chr17:50219800-50221000 Weak transcription HUES48 Cell Line embryonic stem cell
11 chr17:50219800-50221000 Weak transcription NHEK skin
12 chr17:50219800-50222200 Weak transcription HMEC breast
13 chr17:50220800-50221400 Enhancers HUES64 Cell Line embryonic stem cell

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