Tag | Content |
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EnhancerAtlas ID | HS069-07626 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr7:20817100-20818470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr7:20817934-20817954 | CCCCAGACCACCACCTCACT | + | 6.31 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_63362 | chr7:20817781-20839192 | NCI-H69 |
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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: 2 | ID | Chromosome | Start | End |
GH07I020778 | chr7 | 20817241 | 20817390 | GH07I020777 | chr7 | 20817441 | 20818771 |
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Enhancer Sequence | TTCTGTTAGT CCCAGGGTAG CTAAACTTTT TTGATATCCT GAAACTAAAA AGCGCAGAGT 60 TTTCACAGCC AGTCACACTT AATTGCGCCT TCTTTATGAT AACAGTGTGG GGAAATGTGG 120 GCAAGTTCCT TCACTCGTCG AGTCTGCCAA CCCCATGATA AAATGACAAG AATAAATCTT 180 GCCACCTATG GAGGACGCTG CACTTTGACG TCGCTGGGGA GAGGAGGCGG GTGCGAGTGA 240 ACACAAAGCA GTTTGGCCAA GAAAAGAGCA CAGGAGGTGA AGAAAGGCAG GCAGTCGTGG 300 GCCAGGACAG AGAGAAAGCT GAACAAGTTC AGGAAGAAGA ATCTGAGTCT GTCCACGCCG 360 CAGCAGCCTC CGGTGGCACG GGCAGAAAGA TCAAGCGCGG CACCCCGTGA CAGGATGGGA 420 CAGATTCCCC GGGCTCCGAG GCCCTAGGAT GGCGCAGGGC AGCGGGCTGG TGCGGGAAAA 480 CTACAGAGCA AGCGAGGGAG GGAAGCGAAG GCAGGGGAAT CCCTCACCCC GTCCGGCCCG 540 AGTGTCTTTT GAGAGCCCAC AGGCGAGCGG GGCGGGGGGA GGCTCCCCGC GCATTCCCAC 600 CGTGGGTTTG CCCAAGGTCA GAGGCCCGGG ACTGGCGGGG CGGGTCTGGC CGGCATTGCC 660 CGCGCTGAGC GCGCTGCAGA ACGGGAGCAG GGCACAGGGT GGCGCTCGCT GTCCGTGCAG 720 CGGGCGGAGG CGGCCGCGGT GCCTTTGTGT GCGGTGGGCG CGGCGATGGG CTGCTCCGGC 780 CCGCAGCCCG AGGGGAGCGG CGGGCCCGGG CCGGGGCCAG GGCTCGCGGG GAGACCCCAG 840 ACCACCACCT CACTCTTCGC TGCTACGTGC AAGCGGACCG TGCGGATCGC CAGTTCGGAA 900 CCCTCCCCGG GAGGGCCCCG GGGTCTTTCT CAATGTACTG GGCACTTCGA GGAGCTGGGA 960 AGAGGAAAGC GGAGGGTAGC GTTTAGAAAG GGAGGGAAAT CCTCCCAGGC TCAAAACCTC 1020 TCGCAGAATT CATTCGAAAA GAGAACGAAG GGAACTTTGG GCAGGCCGGA CCTCGGCTCA 1080 GCGCCCTGCG AGAGAAGCAG AGGTCGCTGC CAGCGTTTCC TCCCGCGCAG CAAGAAATTG 1140 GTGCCTGAGA AGCAAAGTTG AGGAATGGGC TTTTTAAAAG CGGCAGCCCC AGGCCGGGCG 1200 CGGTGGCTCA CGCCGGTAAT CCCAGCACTT TAAGAGGCCG AGGCTGGCGG ATCACCTGAA 1260 GTCAGGAGTT CGAGACCAGG CCAACATGGT GAAACCGGTC TCTACTGAAA ATGCACAATT 1320 AGCCGGGCGT GGTGGCGGTC GCCTGTAATC CCAGCTACAG GGGAGGCTGA 1370
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