Variant report

Variant rs3729991
Chromosome Location chr11:47368153-47368154
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:47343200-47370600 Strong transcription Primary neutrophils fromperipheralblood blood
2 chr11:47351400-47375600 Weak transcription Primary B cells from cord blood blood
3 chr11:47353600-47375400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
4 chr11:47354000-47369800 Weak transcription Right Atrium heart
5 chr11:47354800-47372800 Weak transcription Gastric stomach
6 chr11:47364000-47370600 Enhancers Fetal Heart heart
7 chr11:47364000-47372200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr11:47364400-47369000 Strong transcription Left Ventricle heart
9 chr11:47364600-47370600 Weak transcription Spleen Spleen
10 chr11:47366800-47368600 Strong transcription Primary monocytes fromperipheralblood blood
11 chr11:47367200-47369200 Genic enhancers Right Ventricle heart
12 chr11:47367200-47372200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr11:47367400-47369800 Strong transcription Monocytes-CD14+_RO01746 blood
14 chr11:47367600-47369000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr11:47367800-47368200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
16 chr11:47367800-47377200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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