Variant report

Variant rs57563765
Chromosome Location chr1:47675352-47675353
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:47659000-47675800 Weak transcription Primary hematopoietic stem cells blood
2 chr1:47664600-47676000 Weak transcription K562 blood
3 chr1:47673400-47675600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr1:47673400-47677600 Enhancers HMEC breast
5 chr1:47673600-47676600 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
6 chr1:47673800-47676000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr1:47674200-47675400 Weak transcription HUVEC blood vessel
8 chr1:47674400-47677200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr1:47674400-47690600 Weak transcription Gastric stomach
10 chr1:47674600-47676000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr1:47674800-47675400 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
12 chr1:47674800-47675400 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
13 chr1:47674800-47675600 Bivalent Enhancer H1 Cell Line embryonic stem cell
14 chr1:47675000-47677200 Weak transcription Spleen Spleen
15 chr1:47675200-47676200 Weak transcription Lung lung
16 chr1:47675200-47676800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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