Tag | Content |
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EnhancerAtlas ID | HS050-50408 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr4:6921600-6922400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr4:6921920-6921935 | TTCTATTTTTGACTC | - | 6.37 | NKX2-5 | MA0063.2 | chr4:6922097-6922107 | CTCAAGTGGT | - | 6.02 | SOX10 | MA0442.2 | chr4:6922001-6922012 | TCCTTTGTTTT | - | 6.32 | Sox3 | MA0514.1 | chr4:6922002-6922012 | CCTTTGTTTT | + | 6.02 | ZNF263 | MA0528.1 | chr4:6921986-6922007 | TCCCCTCCCTTTCTCTCCTTT | - | 6 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_31576 | chr4:6921907-6922397 | Gastric |
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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 |
GH04I006920 | chr4 | 6921908 | 6922397 |
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Enhancer Sequence | CTCCCAAAGT ACTGGGATTA CAGGCGTGAG CCACCGTGCC CGGCCTATTT ATTTATTTTG 60 AAATAGCGTC TCGCTGTGTT GCCCAGGCTG GAGTGCCGTG GCGCTGTCAC AGCTTACTAC 120 TGTCTTGAAC TCCTGGGCTC AAGAGATCTC CCTGCCTCAG CCTTCTCAGT AGCCGGGACT 180 ACAGGTGTGC ACTACCATGC CTGGCTAATT TTTACTTTTG GTAGAGATGG GGGTCTCACT 240 GTGTTGCCCA GGCTGAATCA AATATTTATA TATAGTTGAG TCTATTTCTG AATTCTGCAT 300 TTCATTTAAT TCCTTCACAT TTCTATTTTT GACTCAGCGC TGCACTCTTA CTGGCTCCTT 360 CAATCTCTGG GAAGGAGGGA GATTAGTCCC CTCCCTTTCT CTCCTTTGTT TTTCTGGAGA 420 CAGGATTGTG CCCTGTTGCC CAGGCTGGAG TGCAGTGGTG ATCATAGCTC ATTGCTATGA 480 GTCCTTGAAC TCCTGGGCTC AAGTGGTCCT CCTGCCCCAG CCTCTTGAGT AACTGGGACT 540 ACAGGCATGA GCCACTGCAC CTGGCTCCCC TTTTTCTGCT TTTAATGAAT TTGCTTTTGC 600 TGTGTTGACA CTGAGGCAGG CCAGGCTTCC TAAAGTAGGA GCGTGCAGGC TCCTTACAAA 660 AGCTGACGCC CAAGCAGGAG TGGTTATCAT TCTTTCTTCT GTGCTTGAAA ACCTTCAGCT 720 CCTCTCTGTT TGATGATAGC AGCTACCAAC AAAGTGCCTG TTGGGGGTCA GGTGCCTATT 780 AAATGCTTTT CTTGTGGTAC 800
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