Variant report

Variant rs1876902
Chromosome Location chr10:1196736-1196737
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:1144800-1232600 Weak transcription Right Atrium heart
2 chr10:1194200-1199800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr10:1195200-1197000 Enhancers Primary hematopoietic stem cells blood
4 chr10:1195400-1196800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr10:1195400-1197400 Enhancers Pancreas Pancrea
6 chr10:1195400-1197400 Enhancers Spleen Spleen
7 chr10:1196000-1196800 Enhancers Right Ventricle heart
8 chr10:1196200-1197800 Enhancers Esophagus oesophagus
9 chr10:1196200-1199800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr10:1196400-1196800 Transcr. at gene 5' and 3' H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr10:1196400-1196800 Enhancers Primary T regulatory cells fromperipheralblood blood
12 chr10:1196400-1197000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr10:1196400-1197600 Enhancers Fetal Heart heart
14 chr10:1196400-1198400 Weak transcription Dnd41 blood
15 chr10:1196400-1200600 Weak transcription Ovary ovary
16 chr10:1196600-1197800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr10:1196600-1200400 Weak transcription Fetal Lung lung
18 chr10:1196600-1204600 Weak transcription K562 blood

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