Tag | Content |
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EnhancerAtlas ID | HS051-25327 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr7:101929130-101930570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr7:101930020-101930031 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr7:101930056-101930067 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr7:101930081-101930092 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr7:101930111-101930122 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr7:101929568-101929579 | GGGGGCGTGGT | - | 6.14 | KLF5 | MA0599.1 | chr7:101930021-101930031 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr7:101930057-101930067 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr7:101930082-101930092 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr7:101930112-101930122 | GGGGCGGGGC | - | 6.02 | NHLH1 | MA0048.2 | chr7:101929959-101929969 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr7:101930365-101930375 | CGCAGCTGCG | + | 6.02 | NHLH1 | MA0048.2 | chr7:101929959-101929969 | CGCAGCTGCG | - | 6.02 | NHLH1 | MA0048.2 | chr7:101930365-101930375 | CGCAGCTGCG | - | 6.02 | SP1 | MA0079.4 | chr7:101930019-101930034 | CGGGGGCGGGGCCTG | - | 6.11 | SP1 | MA0079.4 | chr7:101930055-101930070 | AGGGGGCGGGGCCAG | - | 6.57 | SP2 | MA0516.2 | chr7:101930054-101930071 | GAGGGGGCGGGGCCAGG | - | 6.09 | SP3 | MA0746.2 | chr7:101930080-101930093 | GGGGGGCGGGGCC | - | 6.11 | SP3 | MA0746.2 | chr7:101929567-101929580 | AGGGGGCGTGGTG | - | 6.29 | SP4 | MA0685.1 | chr7:101930053-101930070 | GGAGGGGGCGGGGCCAG | - | 7.25 | SP8 | MA0747.1 | chr7:101929567-101929579 | AGGGGGCGTGGT | - | 6.52 | Zfx | MA0146.2 | chr7:101930020-101930034 | GGGGGCGGGGCCTG | + | 6.19 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_58693 | chr7:101922324-101974102 | Ly1 | SE_60412 | chr7:101921972-101976670 | DHL6 | SE_61924 | chr7:101916815-101972690 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 101929153 | 101929600 | chr7 | 101929978 | 101930313 | chr7 | 101929501 | 101929660 |
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Enhancer Sequence | TATCTCCAGG AGCAAGACTA CTCTCTTCTC TGAGCGGCCC TTTCCACACC TCTGCCCCCA 60 CCGAAGCCCT CCCTCCCCTC TCAGACCCCT TCCAGGCCTG CTGAGCCCCC TGCACCTCTT 120 TCAGGAAGCC TCCCAGAGCC CCCGCGCCGT GCCCTCAGCA CCAGGGGTCA GGCTACAAAT 180 GCCCCGCAAA GCCCAGCGGG ACTGTTTCCT CAGCCCCACT GGTCTCTGCC CTAAAGCAGG 240 CGAGTTCTGG AGCCAGGCAG GGGTGAGGAA GGTGCCAGGG TTGTGGCCCC TCATCGCCCC 300 TCTATGATCT CTGACACCTC TCCGGGTGGC ATCAGGCCCC CATCACAGCG AAGGCTGGGT 360 GGTGGGGGCA CTGCGCTCAG GGGGGCCGTC CCGCCCTGTG GCCCGGGGGC GATTTCCCGC 420 ACCGGAGGGC TGCAGGGAGG GGGCGTGGTG GCGCCCTCGA GATTTATGAG AACCAGGCGT 480 CGACTTCCTC CGTTGCGACA TCCAGGCCTC CTCCAGGCTC CCATTGTCCC TGCTGCGGAG 540 AGTCTGGCCA CAGCGGCGGC TCCCGCGAAG CACCCGTCAG CGAGGGGCGC TTCGAGGGCG 600 TCCGCGTCCC ATACACCCGC CACGCAGGAC ATTCCCCCGG CCCCACGCTC CGCGCTCCCG 660 GGGCCACCAC CACCGCGGGC TCGAGGGGTG GCCTCCACGA GGAGGAGTGG GAGTCCCGCG 720 CCTGGCCTGG GGCCGGCTCG GCGACATGGG GACCCCCGCC CAGATGGGGC GACTCGGAGC 780 CGGCTCCTAA CCCCTCTCTC CGGGCCCCAG GACCGGGCAG TCTCGGCACC GCAGCTGCGG 840 GGAGCCAGCA AGCACCGGCC ACCGGCGCCG CTCGGGCTCC GCGGATGGCC GGGGGCGGGG 900 CCTGAGCGGC GCAAGTGGGG GCGGGAGGGG GCGGGGCCAG GACGCGCGAG GGGGGGCGGG 960 GCCGGGGCTC GCGGCGGGGG CGGGGGCGGG GCCGGGGCCG GGAGGCGCGC GCCTCGCGGG 1020 CGGGGGGCGC GCCGCGCTGG GCTGGGCTTG GAGCGCGCGG AGCTCGGCTG CCAGAGAGCC 1080 GCGCGGGGGA CGCGCCGGGA CCGCGAGGAG CGCAGGAGCC TTCGAGGCGG TGAACGAGGG 1140 AGGGAGCCCA GTCCGCCGCG GGCCATGAGC CACCGGGCCC GGGGAGCCCG GCCGCGGTCC 1200 GGGCAGCGCT CAGCCGGCGC CCCAGCCCGC TCGGCCGCAG CTGCGCGCCT GTAGGTATGG 1260 CCTCCTTATA CCCAGTTCCT CGCTCCCTGG TCCTTCCCCC GGGACCCCTG TCTGTCCCCG 1320 GGGACGTGCG CTGTGTGCGC ACCGCTGCCC GAAGGAGAGC GGCCGCACGC GCCTTGGTCC 1380 GCGCGTGTCG TCTTTGTGTG CGCGGGTGGG AGGGAGGAGG GCGCGCGAGG GAGGGGAGGC 1440
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