Variant report

Variant rs17821171
Chromosome Location chr15:58576837-58576838
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:58564400-58582000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr15:58570800-58582200 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr15:58574200-58577400 Enhancers HepG2 liver
4 chr15:58574400-58580200 Enhancers Fetal Thymus thymus
5 chr15:58574800-58577200 Weak transcription Fetal Intestine Small intestine
6 chr15:58574800-58579000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr15:58576000-58577600 Flanking Active TSS Liver Liver
8 chr15:58576400-58577000 Enhancers HSMMtube muscle
9 chr15:58576400-58577400 Enhancers Placenta Amnion Placenta Amnion
10 chr15:58576600-58578400 Enhancers Fetal Intestine Large intestine
11 chr15:58576600-58579800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr15:58576600-58580400 Enhancers Thymus Thymus
13 chr15:58576800-58577000 Enhancers NHEK skin
14 chr15:58576800-58578000 Enhancers Pancreas Pancrea
15 chr15:58576800-58579800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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