Variant report

Variant rs72772800
Chromosome Location chr9:139668400-139668401
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139667600-139669200 ZNF genes & repeats Fetal Intestine Small intestine
2 chr9:139667800-139668400 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
3 chr9:139667800-139668600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr9:139667800-139668600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
5 chr9:139667800-139668600 ZNF genes & repeats Skeletal Muscle Male skeletal muscle
6 chr9:139668000-139668600 ZNF genes & repeats Colonic Mucosa Colon
7 chr9:139668000-139669200 ZNF genes & repeats K562 blood
8 chr9:139668200-139668600 ZNF genes & repeats Fetal Thymus thymus
9 chr9:139668200-139668800 Enhancers Primary B cells from peripheral blood blood
10 chr9:139668200-139682400 Weak transcription Right Atrium heart
11 chr9:139668400-139668600 Flanking Active TSS HepG2 liver
12 chr9:139668400-139668800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --

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