Tag | Content |
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EnhancerAtlas ID | HS120-03069 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr19:934620-935740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZIC1 | MA0696.1 | chr19:935253-935267 | CGCGGCGGGGGGCC | - | 6.1 | Zfx | MA0146.2 | chr19:935107-935121 | CAGGCCTGGCCCGC | - | 6.24 | Zfx | MA0146.2 | chr19:935248-935262 | CAGGCCGCGGCGGG | - | 6.91 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_27633 | chr19:931683-935810 | Fetal_Intestine | SE_28572 | chr19:931612-935811 | Fetal_Intestine_Large | SE_47740 | chr19:934081-935683 | Pancreas | SE_57993 | chr19:932068-935605 | VACO_9m | SE_69171 | chr19:931842-935324 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 934999 | 935434 | chr19 | 934763 | 935400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I000931 | chr19 | 931740 | 935806 |
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Enhancer Sequence | AGGCCCTGAG GTGGACTAAA GCTCGGCTTG TGTGTAGGGA CCGGGTGCCG CCTCTGGGTC 60 TTGCGGGAGA CGGGATTGGA ACTCCGAGAA GATGAGGGCC TAGGGATGGT CGTGGGCAGC 120 GGGGGTGGGG GGAGGCCCCC GCCCTGCAGT CCTGTGACTT TTTTTTCTCT AGAGAAGGGC 180 TTTCACGGTG TTGCCCAGGT TGGTCTCAAA CTCCTGGGCT CAAGTGATCT GCCTCACTCA 240 GCTTCCCAAA GTGCTGGGAT TACAGGCCTG AGCCACGGTG CCCAGCCAGT CCTGGGATCT 300 TATCCTGGGC TGTTCGTGGC AGGTCCAGCC GCCGATGCCG CCGCCCGCCC AGCTGGCCAG 360 ACACCTGTGT TCCCAGTGTC AACAGTGGCC TGGGCCCAAC CAGCCCAGTC AGTGTTACCT 420 CCCGCCCGGC CCCTACTGGG GCCCCTGTTG ACTCTGGCGC CTGCCCCACC CCCTTCCTGG 480 CACGTGGCAG GCCTGGCCCG CTGGCCGGCC GCTTGGCACC GTCTCTGCCT CTTCCTCCCA 540 GGTCCTGGCA GGGCTCGGGG CTAACTTCCG CCTGCAAATC CTCGACAGCT GTGAAATTCT 600 GCTGTCGGCT GCAGGTCTGG TGGGTGGCCA GGCCGCGGCG GGGGGCCGGG CGCAGCAGGC 660 TCAGGGCCAC GGGTTCTTTC CTTGGACACC TGGAACCTTG CTGCCTGGGG CCTGGGGACG 720 TGCAGTTTTG GAGGCCAGCA CGTGTCGGGC AGTGATTAGG ATCTCAGCCT CCTGATGTCT 780 GACGTAGCCT CCTGGTGGCC TCCTGTCACC CACACAGCAG GCCCAGCTTC TAGAAAGCGG 840 CCACGGTAGG ATTTTATTGG ATTATTATTA TTTTTGAGGC AGGGTCTTAC TCTGTCGGGT 900 AGGCTGGAGT GTAGTGGTGC TGTCCTAACT CACTGCAGCC TCGATCTCCT GGGTTCAAGC 960 GATCCTTCTG CCTCAGCCTC CTGAGTAGCT GCGAGTACAG ACGGGCGCCA CCAAACTCAG 1020 CTAATTTTTG TAGAGACGGG GTCTTGCTAT GTTGCCCAGG CTGGTCTAGA ACTCCTGGGC 1080 TCAGGTGATC TGCCCTCCTT GGCCTCCCAA AGTGCTGGGA 1120
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