Variant report

Variant rs6560642
Chromosome Location chr9:139604777-139604778
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139593800-139605600 Weak transcription Liver Liver
2 chr9:139596200-139606200 Weak transcription Fetal Intestine Small intestine
3 chr9:139596400-139606200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr9:139596400-139606200 Weak transcription Spleen Spleen
5 chr9:139600200-139606000 Weak transcription Adipose Nuclei Adipose
6 chr9:139600800-139605000 Weak transcription Primary hematopoietic stem cells blood
7 chr9:139600800-139605000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr9:139603000-139606000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr9:139603000-139606000 Weak transcription K562 blood
10 chr9:139603800-139604800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr9:139604200-139605000 Weak transcription A549 lung
12 chr9:139604400-139604800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin01 Skin
13 chr9:139604400-139605000 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr9:139604400-139606000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
15 chr9:139604600-139604800 Bivalent Enhancer H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr9:139604600-139604800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr9:139604600-139604800 Flanking Bivalent TSS/Enh Foreskin Fibroblast Primary Cells skin02 Skin
18 chr9:139604600-139604800 Flanking Bivalent TSS/Enh HepG2 liver
19 chr9:139604600-139605000 Flanking Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
20 chr9:139604600-139606200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
21 chr9:139604600-139606400 Enhancers Hela-S3 cervix

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