Variant report

Variant rs232841
Chromosome Location chr1:59040178-59040179
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:59035800-59041000 Enhancers Primary neutrophils fromperipheralblood blood
2 chr1:59038000-59040200 Enhancers HUES48 Cell Line embryonic stem cell
3 chr1:59038000-59041200 Weak transcription Brain Substantia Nigra brain
4 chr1:59038200-59040200 Flanking Active TSS NHEK skin
5 chr1:59038400-59043600 Active TSS Breast Myoepithelial Primary Cells Breast
6 chr1:59038600-59040200 Flanking Active TSS GM12878-XiMat blood
7 chr1:59038600-59041200 Enhancers Hela-S3 cervix
8 chr1:59038800-59040200 Enhancers Fetal Lung lung
9 chr1:59038800-59040600 Enhancers HUVEC blood vessel
10 chr1:59039000-59040200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:59039200-59040200 Enhancers Primary T helper memory cells from peripheral blood 1 blood
12 chr1:59039600-59040200 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr1:59039600-59041000 Flanking Active TSS HMEC breast
14 chr1:59039600-59041200 Active TSS Esophagus oesophagus
15 chr1:59039800-59040800 Enhancers Placenta Amnion Placenta Amnion
16 chr1:59040000-59040200 Bivalent Enhancer Primary T helper 17 cells PMA-I stimulated --
17 chr1:59040000-59040400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr1:59040000-59041200 Bivalent Enhancer Monocytes-CD14+_RO01746 blood
19 chr1:59040000-59041800 Active TSS Pancreas Pancrea
20 chr1:59040000-59042000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
21 chr1:59040000-59042000 Active TSS Stomach Mucosa stomach

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