Variant report

Variant rs17115551
Chromosome Location chr1:85250955-85250956
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85241000-85263600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:85248000-85251200 Weak transcription Fetal Heart heart
3 chr1:85250200-85251800 Enhancers Stomach Smooth Muscle stomach
4 chr1:85250400-85252000 Enhancers Breast Myoepithelial Primary Cells Breast
5 chr1:85250400-85252000 Enhancers Rectal Smooth Muscle rectum
6 chr1:85250600-85251400 Enhancers Brain Cingulate Gyrus brain
7 chr1:85250600-85251800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr1:85250600-85251800 Enhancers Colon Smooth Muscle Colon
9 chr1:85250600-85251800 Enhancers HMEC breast
10 chr1:85250800-85251200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr1:85250800-85251200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:85250800-85251400 Enhancers NHEK skin
13 chr1:85250800-85251600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr1:85250800-85251600 Enhancers Brain Hippocampus Middle brain
15 chr1:85250800-85251800 Enhancers Fetal Stomach stomach
16 chr1:85250800-85252400 Enhancers Fetal Lung lung

Quick Search:


  
Input of quick search could be:

what's new

Quick links