Variant report

Variant rs55936451
Chromosome Location chr1:173033519-173033520
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173030800-173033600 Enhancers Fetal Lung lung
2 chr1:173031800-173033600 Weak transcription Placenta Amnion Placenta Amnion
3 chr1:173032400-173034400 Enhancers HUVEC blood vessel
4 chr1:173032800-173033800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:173032800-173033800 Enhancers HMEC breast
6 chr1:173033000-173033600 Enhancers Colon Smooth Muscle Colon
7 chr1:173033000-173033800 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr1:173033000-173033800 Enhancers Placenta Placenta
9 chr1:173033000-173033800 Enhancers NHLF lung
10 chr1:173033000-173034000 Enhancers Adipose Nuclei Adipose
11 chr1:173033200-173033600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
12 chr1:173033200-173033600 Flanking Active TSS NHEK skin
13 chr1:173033200-173033800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr1:173033200-173033800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr1:173033200-173033800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr1:173033200-173033800 Enhancers Rectal Smooth Muscle rectum
17 chr1:173033400-173033600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
18 chr1:173033400-173033800 Enhancers Esophagus oesophagus

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