Tag | Content |
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EnhancerAtlas ID | HS177-18559 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr5:141444780-141445340 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr5:141445058-141445074 | TGTTGCTATGGCAACT | + | 6.78 | RFX1 | MA0509.2 | chr5:141445058-141445074 | TGTTGCTATGGCAACT | - | 6.78 | RFX2 | MA0600.2 | chr5:141445058-141445074 | TGTTGCTATGGCAACT | - | 7.13 | RFX2 | MA0600.2 | chr5:141445058-141445074 | TGTTGCTATGGCAACT | + | 7.16 | RFX5 | MA0510.2 | chr5:141445058-141445074 | TGTTGCTATGGCAACT | - | 7.37 | RFX5 | MA0510.2 | chr5:141445058-141445074 | TGTTGCTATGGCAACT | + | 7.43 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I142063 | chr5 | 141442808 | 141444824 |
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Enhancer Sequence | TAGGTAAACA TGTGTCATGG GGGTTTGTTG TTCAGATTAT TTCATCACCC AGGTATTAAG 60 CCTAGTACCT GTTAGTTATT TTTCCAGATC CTCTTCTTAA GATTTTCAAG TGAGGAAGTG 120 AAATGAGGGT GGAAAGGCAG AGGAGGGTGC TTTGCTTAGA GACCAGGACA GGTCAGAGAC 180 AGGGCATAGG CACAGCTGTG GACTGACCAC CCCCTGCCTC CCCAGCCAGA AGTGCCGGGA 240 AATGCAGACA TCCCTATTTG GACTCTGGTG CAGTCCTCTG TTGCTATGGC AACTCAGGGG 300 CTCTGTGGTT GGTGGAAGAA GGCAGTGGCT GTGTGGAAAT CGGCATTGGA GGCAGCAGCT 360 GTGCCCTTTT GCTCCAGCAG TCTGGGTATT TCTGATGGGG GCAGGGTGGG GATACTCCCT 420 CTGCCATCTC AGGAAGCCAC ACAGGAGACC CCTGGACTCC ACGGCCAATG CCTCTGGCTC 480 AGATCAGCTC CCACCCAGAC TCCCTCACAG GGAGGAACCA GGCTTCTGTA TGGAGTGGCA 540 ATTCCCTTGG CACCCCTACC 560
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