Tag | Content |
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EnhancerAtlas ID | HS062-15200 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr7:101185580-101187040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZEB1 | MA0103.3 | chr7:101186327-101186338 | GCGCAGGTGGG | - | 6.62 | Zfx | MA0146.2 | chr7:101185627-101185641 | CCCGCCTCGGCCTC | + | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 101185880 | 101186571 | chr7 | 101186720 | 101186956 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I101542 | chr7 | 101186181 | 101186350 |
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Enhancer Sequence | ACCATGTCGG CCAGGCTGGC CTCAAACTCC TGACCTCAAG TGATCCACCC GCCTCGGCCT 60 CCAAAGTGTG GAATTACAGG TGTGAGCTAG CGCACCCAGC CTACAGATAT CACTCTTAAT 120 CTTCACACAA AGCTTGGAAG CCTTGAGGTT ACAGGGGAGA CACCTGAGGC TCAGAGAAGT 180 TAAGTGACAC CCCTGGGGTC ACCCAGCAAG CCAGCAAGCT GGGGGCATTT TGCCTCCATG 240 ATTCTCTGCC CTTAGAGCCC TTTGGAGGGG GCGCTCTCCC TCTGCCCTCT GTTCTGAGTG 300 TCTATTCTGA TGCTGGGTTG GGGAGCAGGG GCAGAGCAGG GAGGAGAGAT GCATGACACA 360 GGTGGCCTCC AGTGGCCAGT CCCAGGGCCG GGGAAGGAGA GTAGGGTATC CTGCATTCTT 420 GGAAAGGGAC TGAAGGCTGC GGGAGGAGGG CCGAGCTCAG GTCTCCTACG GGAAGGGGGA 480 CCTCTCTCAC TCTGGCCCCC GGCCTACCCC TCGAGCCGCT GTCCCTAAGG TCTCACCCCC 540 AGAGCGTTAC CTCATGCCCA CATTCTTCAG ATCTTTCTTG GGGGATGGAG GAGGAGGGGC 600 TTCCCATCCC ACCGGGGACC CAGGCCCACG AAAGCGCATG CCTGGCAAGA CCTTTCCAAC 660 CAGGGGAAAA TGCAGTTTCA AGAATGGCCA CCAGGTGGGG CACACACTCT ACACATGGTG 720 ACACCTGCAG CCAACCTGGA TTCCAGAGCG CAGGTGGGGC TCTTCCGAGG CCAGCAGCCC 780 CCAGCCAGGC CCTCCCCACC ATACCACAGT CCCATGCAGG CAGAGTGCAA AGGGCCCTAA 840 GACTCAGTGC AGGTCCCTTC ATCAGATCAG CAAACTTTTT TTTTTTTTCT GAGACGGTCT 900 CGCTCTGTAA GCCAAGCTGG AATGCAGTGG TGTGATTATA GCTCACTGCA GCCCAGACCT 960 CCTGGGCTCA AGCCATCCTC CCACCTCAAC GTCCCCAGTA GCTGGGGCCA CAGGCGTGCA 1020 CCACTATGCC CGGTTAACTT TTGTATCTTT TGTAGAGATG GGGTCTCACT ATGTGGCCCA 1080 GGCTGGTCTC AAACTCCTGG GCTCAAGTGA TCTTCCTGCC TCAGCCTCCT AAGGTGCTGA 1140 GCAAACATTT TTCAGCATCC TCTCTGGGCC AGAGGGAGAA AAGGCTGTCC CCTGGCCACA 1200 CAGCAAGCCT TACCTCTCCA TCTCCTTGTC CACCCTTGGG GTTTAGAGAT CTGTAGCTGG 1260 GAAGATCCAT CCTTCAGGAC CTCCTGGGGC CTCCTCGGAG GCCACCTGTT GGGGAGCACT 1320 TTGCCACAAG CCCGGTTCTT GACCCTAAGC AGAGAGACAG CAGGGTGTGA GAGAGGGACC 1380 TGGAGCTAAG CAACTTCATC TGCAGCCTGG CTGTGTGAGC TTGGGCAAGG GACCAACCTT 1440 CCTGAGCCTC AGTTTCCCCA 1460
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