Variant report

Variant rs4926808
Chromosome Location chr1:47572203-47572204
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47557800-47573800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:47570600-47573600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr1:47570800-47572400 Weak transcription NHEK skin
4 chr1:47570800-47573200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:47572000-47573400 Enhancers Liver Liver
6 chr1:47572200-47572400 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr1:47572200-47572400 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr1:47572200-47572400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr1:47572200-47573000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:47572200-47573600 Enhancers HUES48 Cell Line embryonic stem cell
11 chr1:47572200-47573600 Enhancers HUES64 Cell Line embryonic stem cell
12 chr1:47572200-47573800 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr1:47572200-47574400 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr1:47572200-47574800 Enhancers HMEC breast

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