Variant report

Variant rs1847222
Chromosome Location chr1:47572843-47572844
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr1:47570800-47573200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:47572000-47573400 Enhancers Liver Liver
5 chr1:47572200-47573000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:47572200-47573600 Enhancers HUES48 Cell Line embryonic stem cell
7 chr1:47572200-47573600 Enhancers HUES64 Cell Line embryonic stem cell
8 chr1:47572200-47573800 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr1:47572200-47574400 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr1:47572200-47574800 Enhancers HMEC breast
11 chr1:47572400-47573000 Weak transcription iPS-20b Cell Line embryonic stem cell
12 chr1:47572400-47573000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr1:47572400-47573000 Enhancers Hela-S3 cervix
14 chr1:47572800-47573400 Enhancers HUVEC blood vessel
15 chr1:47572800-47573600 Flanking Active TSS ES-I3 Cell Line embryonic stem cell
16 chr1:47572800-47573600 Flanking Active TSS NHEK skin

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