Variant report

Variant rs7745722
Chromosome Location chr6:146014776-146014777
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:146003400-146033600 Weak transcription Brain Hippocampus Middle brain
2 chr6:146003600-146020600 Weak transcription Primary T helper cells fromperipheralblood blood
3 chr6:146003600-146029400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr6:146003800-146026600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr6:146003800-146029600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr6:146003800-146029600 Weak transcription Ovary ovary
7 chr6:146006800-146014800 Weak transcription Adipose Nuclei Adipose
8 chr6:146006800-146050000 Weak transcription Brain Cingulate Gyrus brain
9 chr6:146007000-146022400 Weak transcription Primary B cells from cord blood blood
10 chr6:146007400-146043800 Weak transcription Liver Liver
11 chr6:146008600-146015600 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr6:146009600-146022400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr6:146011200-146020000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr6:146011200-146029600 Weak transcription Aorta Aorta

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