Variant report

Variant rs10867084
Chromosome Location chr9:140774721-140774722
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:140773200-140795400 Weak transcription Right Atrium heart
2 chr9:140773800-140774800 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr9:140773800-140775400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr9:140773800-140777000 Weak transcription HUES64 Cell Line embryonic stem cell
5 chr9:140773800-140777000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr9:140774000-140774800 Bivalent Enhancer Brain Cingulate Gyrus brain
7 chr9:140774000-140775000 Transcr. at gene 5' and 3' Fetal Brain Female brain
8 chr9:140774000-140775200 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr9:140774000-140775600 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr9:140774000-140776400 Enhancers Fetal Brain Male brain
11 chr9:140774000-140777200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr9:140774400-140774800 Bivalent Enhancer Brain Inferior Temporal Lobe brain
13 chr9:140774600-140774800 Flanking Bivalent TSS/Enh Brain Dorsolateral Prefrontal Cortex brain
14 chr9:140774600-140775800 Genic enhancers Brain Germinal Matrix brain

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