Variant report

Variant rs1876900
Chromosome Location chr10:1197018-1197019
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr10:1195400-1197400 Enhancers Pancreas Pancrea
4 chr10:1195400-1197400 Enhancers Spleen Spleen
5 chr10:1196200-1197800 Enhancers Esophagus oesophagus
6 chr10:1196200-1199800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr10:1196400-1197600 Enhancers Fetal Heart heart
8 chr10:1196400-1198400 Weak transcription Dnd41 blood
9 chr10:1196400-1200600 Weak transcription Ovary ovary
10 chr10:1196600-1197800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr10:1196600-1200400 Weak transcription Fetal Lung lung
12 chr10:1196600-1204600 Weak transcription K562 blood
13 chr10:1196800-1197600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr10:1196800-1206600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
15 chr10:1197000-1197400 Enhancers NHEK skin
16 chr10:1197000-1200000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
17 chr10:1197000-1200600 Weak transcription Primary hematopoietic stem cells blood

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