Variant report

Variant rs913277
Chromosome Location chr9:96910136-96910137
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:96903000-96912000 Weak transcription HepG2 liver
2 chr9:96903800-96910800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr9:96904000-96912800 Weak transcription NH-A brain
4 chr9:96904000-96927200 Weak transcription Thymus Thymus
5 chr9:96904400-96912600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr9:96904600-96913200 Weak transcription Adipose Nuclei Adipose
7 chr9:96904800-96910200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr9:96904800-96912000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr9:96904800-96912000 Weak transcription Spleen Spleen
10 chr9:96906800-96911000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr9:96907200-96912200 Weak transcription Fetal Muscle Leg muscle
12 chr9:96907400-96913200 Weak transcription Lung lung
13 chr9:96909000-96910600 Enhancers NHEK skin
14 chr9:96909400-96913000 Weak transcription Placenta Amnion Placenta Amnion
15 chr9:96910000-96910400 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr9:96910000-96911000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
17 chr9:96910000-96911000 Enhancers Esophagus oesophagus

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