Variant report

Variant rs16848575
Chromosome Location chr1:175499050-175499051
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:175489600-175500000 Weak transcription Brain Substantia Nigra brain
2 chr1:175491200-175499400 Weak transcription HMEC breast
3 chr1:175494800-175505600 Weak transcription Spleen Spleen
4 chr1:175496200-175499800 Weak transcription Liver Liver
5 chr1:175496800-175501200 Enhancers NHEK skin
6 chr1:175497000-175501200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:175497200-175501800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr1:175498000-175500200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:175498200-175500400 Enhancers Fetal Muscle Leg muscle
10 chr1:175498200-175500600 Enhancers Brain Germinal Matrix brain
11 chr1:175498200-175502000 Enhancers Cortex derived primary cultured neurospheres brain
12 chr1:175498400-175499400 Weak transcription Fetal Brain Male brain
13 chr1:175499000-175500400 Enhancers Fetal Brain Female brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links