Variant report

Variant rs73579478
Chromosome Location chr6:146011790-146011791
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:145995200-146013200 Weak transcription Pancreas Pancrea
2 chr6:146001800-146012200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
3 chr6:146003400-146033600 Weak transcription Brain Hippocampus Middle brain
4 chr6:146003600-146020600 Weak transcription Primary T helper cells fromperipheralblood blood
5 chr6:146003600-146029400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr6:146003800-146012200 Weak transcription Primary hematopoietic stem cells short term culture blood
7 chr6:146003800-146012400 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr6:146003800-146026600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr6:146003800-146029600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr6:146003800-146029600 Weak transcription Ovary ovary
11 chr6:146006800-146014800 Weak transcription Adipose Nuclei Adipose
12 chr6:146006800-146050000 Weak transcription Brain Cingulate Gyrus brain
13 chr6:146007000-146022400 Weak transcription Primary B cells from cord blood blood
14 chr6:146007400-146043800 Weak transcription Liver Liver
15 chr6:146007800-146013600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr6:146008600-146015600 Weak transcription Skeletal Muscle Male skeletal muscle
17 chr6:146009600-146022400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
18 chr6:146010000-146012200 Weak transcription HUES64 Cell Line embryonic stem cell
19 chr6:146011000-146012000 Weak transcription HepG2 liver
20 chr6:146011200-146020000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
21 chr6:146011200-146029600 Weak transcription Aorta Aorta

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