Tag | Content |
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EnhancerAtlas ID | HS111-02463 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr19:1226660-1227590 |
Target genes | Number: 31 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr19:1227044-1227064 | TGGTGGGTGGTGGGGAGGGG | - | 6.3 | RREB1 | MA0073.1 | chr19:1227041-1227061 | GGGTGGTGGGTGGTGGGGAG | - | 6.63 | Stat4 | MA0518.1 | chr19:1226989-1227003 | CTTCCAGGAAAGGC | + | 6.02 | Zfx | MA0146.2 | chr19:1227060-1227074 | GGGGCCGCGGCCTC | + | 6.59 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I001227 | chr19 | 1227316 | 1228274 |
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Enhancer Sequence | AGGTGGGGCG CGGCGGGGCC CGGGTGGGGC ATGTGGGGAC AACGCCTGGA TGCCACAGCC 60 AGCCGTGAGC ATAGCCCGCG CTAGTCAGTC ATGGTGACCG TCACGTGGCT GCGCGTGGTT 120 GCCATGTGGC CTTTGGGTGG CTTGGCCACG TAGCGATCCC CGTGGAGGGT GCCGTCTCGG 180 GGCCTGGTGT CTGGCCAGCG TGCTGGTCAT GGAGGCCTAC GTGTGGCGGG GCTCTGGGGG 240 GGCGTGCCGT CCTCACAGCC ACCTCTCAGA GTGGGTGCAT TCCGAGGACC CTGCCCTGGG 300 CCTGGCGCCC CCTCCCCATG CCCGCGCCGC TTCCAGGAAA GGCTTATGCT GGGCTCAGCC 360 CAGAGGCTTT TGAGCACCAG TGGGTGGTGG GTGGTGGGGA GGGGCCGCGG CCTCCATGGC 420 TCTGCCGGGG TGCCGCAGGC TCTGAGCCAG CTGCCAAGTA TGGCTGAGGC TGAGTCGTGC 480 CGGACGCTGC CCTGTCTCTC CCTGTGTGCC TGCCTCCTCT CCCAGCCCCA GCCCCAGCCC 540 CGGGTGGGAG ACGGAGTCCC AGAGGTGTCA GAGACCCTTA AGTCACCTGC CGAGGATGCG 600 GGGTGGATGG GGGCCCGAGG CTGAAGCCCC TGCCTTGCCA CAGCCCCTCT CCCAGGTTTT 660 GGGGGCCACC GCCTGAGTTA CATGTCTGTC CCCCAAATGG GTGCCCACAG CCCATCCACC 720 AGCGTCAGAG CCCGCCAGGC CCCACTGCAA AAGGCCACAC AATGTACCCC GGGAGTGACT 780 CAAGGGTGGC CTTCCCTGGC CTCCCCTGCT GCCCCCCAGG AGTCCGGTAG CCCCATGACT 840 GTACCTCAGC TTCTCCATCC TCCCAGGGGC CCGCGGGAGG CGGAGAACCG GTGCCCAGGC 900 TGACCTCTTC CGTCTTCCTT CCACCCTGCA 930
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