Tag | Content |
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EnhancerAtlas ID | HS051-24470 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr7:1208940-1210060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr7:1209683-1209702 | CAGCTCCCCCTGGCGGCAG | - | 6.09 | INSM1 | MA0155.1 | chr7:1209642-1209654 | CGCCCCCTTGCA | - | 6.02 | KLF14 | MA0740.1 | chr7:1209637-1209651 | GGCCACGCCCCCTT | + | 8.42 | KLF16 | MA0741.1 | chr7:1209638-1209649 | GCCACGCCCCC | + | 6.62 | SP1 | MA0079.4 | chr7:1209635-1209650 | CCGGCCACGCCCCCT | + | 6.19 | SP3 | MA0746.2 | chr7:1209637-1209650 | GGCCACGCCCCCT | + | 6.82 | SP4 | MA0685.1 | chr7:1209635-1209652 | CCGGCCACGCCCCCTTG | + | 6.59 | SP8 | MA0747.1 | chr7:1209638-1209650 | GCCACGCCCCCT | + | 6.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35540 | chr7:1208673-1210137 | HepG2 |
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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 |
GH07I001169 | chr7 | 1208950 | 1210250 |
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Enhancer Sequence | GTGGGGAGTC ACCTGTCTGC CAGGCTGGAC GGGTGAACAC ATTCATCATC TTTAGGCATG 60 CGAGCTTCTC CTACCTCTAT CCATCCTTCC TTCAGCCCAT TTCCCCCGAC TTCTGCCACC 120 ACCTCCGGGA CGTCCTGAAG GCGAACCGGC CTCCCACCTG CTAAGTCCAA CAGACACTTC 180 AGCCTGGCTC TCACCAGCCA TGGCGGGTTG CCCTCCTACC TCTTGACAAC ACGCTCTTCC 240 TCGGCTGCAG AGACACCTCC TCTCCGTATT TTCCTCCCAC ATTAGCAATG ACCACACTCA 300 GGCTATGTCA CTCATGGTAT TTTTGCATCA GAAATGCCAT CCTTGGGCCG GGCGCCATGC 360 CTCATGCCTG TAATCCCAGC GCTTTGAGAG GCCGAGCCGG GTGGATCCCT TGAGGCCAGG 420 AGTTCAAAAA CGGCCTGGGC AACATAGCAA GACCCTGTCT CTACAAAAAG AAACAGTTTT 480 TAAGTCATTC CTGATTTTAC AACGCTACTC TGATCTGAGC CCCTGTGGCC TCGGGATCCC 540 CAGGCGTCTG TTCCCGAGAA CGCGGGGCAG AAAGCCTAGT CCTGCACGCA GTACCAACAA 600 TGCGGAGTCA GCGGGTTGTT TCGACTTTGT TCTGTTTCCT GAGGGGTTCT GAATAAGGGC 660 CACCCCCTTC CTCCTCTGTG CCGCCATGTT CCCTCCCGGC CACGCCCCCT TGCAACCCCT 720 CCAATCTCCG CCCTGCACCC TGGCAGCTCC CCCTGGCGGC AGCAGCGGGT CTTCGTGGAG 780 TCAGCCCCTC CGCTGCTTGG CCGCTGGGTT TGTCCCTTAT TTTAATGGAT GCGCGTTGGC 840 TAGGACTGCA ACATTGTTTC TTTCTTCCAC AAATTTTAGT TTGAAACAGA CAGGAAGTTA 900 ATTTCCCGTC TGGCTGCCAC ACCTGCTGGT GGCGTGGACT GCGGCCCTTA GGCTGTTCCT 960 TGCTCGATTT AACCCTGGGA GACATCGAAG CCTTCCCACC CAAGCTGTAG GGAGCTGTTG 1020 AAGACCTGGT TCACACGAGA TCCTTTGCGG GGTGCAGCTG GGGAAAGCAT GATTTCAGCT 1080 TGTAAGCTGC ATGGAGAATG CAAATGTATG TGTGTGTGTA 1120
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