Tag | Content |
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EnhancerAtlas ID | HS120-03178 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr19:9895870-9897040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP1 | MA0079.4 | chr19:9896387-9896402 | CAGACCCCGCCCCCA | + | 6.25 | SP4 | MA0685.1 | chr19:9896387-9896404 | CAGACCCCGCCCCCATC | + | 6.43 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_28527 | chr19:9894046-9897642 | Fetal_Intestine |
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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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Enhancer Sequence | CCGAGATTTT TTTTTTTTTT TTTTTTTGAG ACGGAGTCTC GCTCTATCAC CAGGCTGGAG 60 TGGCCCGATC TCGGCTCACT GCAACTTCCG CCTCCCAGGT TCAAGCGATT CTCCTGCCTC 120 AGCCTCCCCA GTAGCTGGGA CTACAGGCGC CTGCCAGCAT GCCCAGCTAA TTTTTGTATT 180 TTTAGTAGAG ATGGGGTTTC ACCATGTTGG CCAGTATGGT CTTAATCGAT TGCCCTCGTG 240 ATCCGCCTGC GTCAGCCTCC CAGTCTGTCC CCTCACCACT ACTCTCTTTC ACGGAGACCC 300 CACCCCCATC TCTCCCTTCA CCGACTCCCC GCCCCCGTCT CTCGCTCACG GAGTCCCCGC 360 CCCTGTCTCA ACCAAGACCG AGTCCCCGCC CCCATCTCTC CCTCGCCGAG TCGCCGCCCG 420 CGTCTCTCCC TCACCCAGAC CCCGCCCCAT CTCTCCCTCA CCGAGACCCC GCCCCATCTC 480 CCCCTCACCG AGACTCCGCC CCCGTCTCTC CCTCACCCAG ACCCCGCCCC CATCTCCCTC 540 TCACCGAGTC CCCGCCCCCA TCTCTCCCTC ACCAAGACCT TGCCCCCATC TCCCCCTCAC 600 CGAGGCTCCG CCCCCGTCTC ACCCTCACCG AGACCCCACC CCCATCTCGC CCTTCACCCA 660 GTCCCCGCTC CCATCTCTCC CTCACCGAGA CCCCGCCCCC GTCTGCCTCC CTCCGGGTGG 720 CTAAGCCGCA CCTGAAGCCG CACCTGGTCG CAGAGGCTAC TGCTGGGGAA ACCGTTGGGC 780 CAGCGGCGGC TAAAGGGCAG GAGGCGCCGC TGTGGCCACG CGCACTTCTG ATTCCGCTCC 840 AGGGTTTCAG AAGGAACTGA GGGCTCTGGA CCCGGCCTCG GAGGCCTGAG GAGTTGGGAG 900 GGGCGGCGGC CGCGTCCTCC GCAACTCTGG GGAGAAGTCT TAGTTTCCGC GCAGCCAAAC 960 GCGATTGGAC CCCGCCCTCC GGCTTCACTG GGGACCGTGG GGGCGGAACC CGGCGGGAGG 1020 ACGTATGGGG GGCTGGACCA TGATGGAGGG AGTCGGTTGG GCTGGACCTC GAAATGCCTC 1080 TGCTCGCTTT CCTCTGCGCT TATGCCGCCA TGTACGAGTA TGCGCTGTTT CCAGGTGGTT 1140 TGTTATACAG CAGTAGATAA CTGATACATC 1170
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