Variant report

Variant rs13374288
Chromosome Location chr1:220500106-220500107
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:220498400-220500200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr1:220498800-220500200 Enhancers GM12878-XiMat blood
3 chr1:220498800-220503000 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr1:220499000-220500200 Enhancers NH-A brain
5 chr1:220499000-220501600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr1:220499000-220502600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr1:220499000-220509400 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr1:220499200-220500600 Weak transcription Esophagus oesophagus
9 chr1:220499600-220500400 Enhancers Placenta Amnion Placenta Amnion
10 chr1:220499600-220500600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr1:220499800-220500200 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:220499800-220500200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:220499800-220500200 Enhancers NHEK skin
14 chr1:220499800-220500600 Enhancers Skeletal Muscle Male skeletal muscle
15 chr1:220499800-220500800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr1:220500000-220500600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
17 chr1:220500000-220501800 Weak transcription ES-WA7 Cell Line embryonic stem cell
18 chr1:220500000-220502600 Weak transcription iPS-20b Cell Line embryonic stem cell

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