Variant report

Variant rs7744082
Chromosome Location chr6:146019798-146019799
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr6:146006800-146050000 Weak transcription Brain Cingulate Gyrus brain
8 chr6:146007000-146022400 Weak transcription Primary B cells from cord blood blood
9 chr6:146007400-146043800 Weak transcription Liver Liver
10 chr6:146009600-146022400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr6:146011200-146020000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr6:146011200-146029600 Weak transcription Aorta Aorta
13 chr6:146016000-146026800 Weak transcription Skeletal Muscle Male skeletal muscle
14 chr6:146019200-146020600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
15 chr6:146019400-146019800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr6:146019400-146020400 Enhancers Muscle Satellite Cultured Cells --
17 chr6:146019400-146021400 Enhancers NH-A brain

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