Variant report

Variant rs11211450
Chromosome Location chr1:47573206-47573207
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr1:47572000-47573400 Enhancers Liver Liver
4 chr1:47572200-47573600 Enhancers HUES48 Cell Line embryonic stem cell
5 chr1:47572200-47573600 Enhancers HUES64 Cell Line embryonic stem cell
6 chr1:47572200-47573800 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr1:47572200-47574400 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr1:47572200-47574800 Enhancers HMEC breast
9 chr1:47572800-47573400 Enhancers HUVEC blood vessel
10 chr1:47572800-47573600 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
11 chr1:47572800-47573600 Flanking Active TSS NHEK skin
12 chr1:47573000-47573600 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr1:47573000-47573600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr1:47573000-47573600 Flanking Active TSS Hela-S3 cervix
15 chr1:47573200-47573600 Flanking Active TSS HUES6 Cell Line embryonic stem cell
16 chr1:47573200-47574800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr1:47573200-47578000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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