Tag | Content |
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EnhancerAtlas ID | HS093-11047 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:391940-393940 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr16:391965-391980 | AAACGCACCAATCAG | + | 6.73 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr16 | 392658 | 392775 | chr16 | 392396 | 392510 | chr16 | 392275 | 392350 | chr16 | 392055 | 392128 | chr16 | 392651 | 393129 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I000342 | chr16 | 392161 | 393428 |
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Enhancer Sequence | GCTTTGTGTC TAGCTCAGGG ATTGTAAACG CACCAATCAG CGCCCTGTCA AAACAGACCA 60 CTGGACTCTA CCAATCAGCA GGATGTGGGT GGGGCCAGAT AAGAGAATAA AAGCTGGCTG 120 CGGGAGCCAG CAGTGGTAAC TCGCTCGGGT CCCCTTCCAT AGTGTGGAAG CTTTGTTCTT 180 TCTCTCTTTC CAGTAAGTCT TGCTGCTGCT CACTCTTTGG GTCCACACTG CCTTTATGAG 240 CTGTAACACT CACCGCGAAG ATCTGCAGCT TCACTCCTGA AGCCAGTGAG ACCACGAACC 300 CACCAGAAGG AAGAAACTCC GAACACCTCC GAACGTCAGA AGGAACAAAC TCCGGACAGG 360 CCGCCTTTAG GAACTGTAAC ACTCACGGCA AGGGTCCGCG GCTTCATTCT TGAAGTCAGT 420 GAGACCAAGA ACCCACCAAT TCCGGACACA CCGGGACGAC TAACCGGCTC TCCACAGGAT 480 ATGCATCCCC TAACACGTGA GGCCTAAGCT CCAGGCCCTG CTGTGGTAGC AATGCTCACC 540 AGCCGCCTGT TCAGTACCCA CTCTCCTTTT CCCTTTGCAT TACCCGCAGC CTTCCTTTGG 600 AGGACTGCCC CCAGCTCCCC ACTGGGGAGC AGCCGTCTGT CTGGGTGGAG AACCCACTTT 660 CCTTCAGGAG TGACCCTGCT GCACAGCCCC CAGCGCACGC ACCGTGACTG TGCTGAGACA 720 GACGGGACAC AGCGGCACAC GTGCCCTCCT CAGAGCAACA GCGGGCCCAT CCGTCAGAGC 780 TGCGGGAAGC ATCTGTAAAC AAGGGAGCCC AGAGCCCAAG GTCACTGCAG CAGCCACCTC 840 CAACACAAAG CCCACGAAGT CGCCCACCAG GCAGGCAAAG TCAGAATGGC ACAAAGCAAA 900 GGTGCCAGGC CCTAAGGCAC ACCTGAGGCT CTGCCTCAAC AGTGCCCTTC AGGGTTGGGC 960 TCAGGTGGGT GGGTTTCCAC GACTTCCAAC CTAGTGCACC CTCACCTACA CCTGGCAGGA 1020 CAAAGAGAAT GGTCTAAATG TGAGGAACGC AGCCTGGACT TCATGCCCTG TCTGTGCTGA 1080 CAAGCAACCA TTCCAACATC AGAGATCTTC AAGCCACAAG GCTGCACCAC AGGCCACCTC 1140 CCACAGAGAG GATTCAACCG CAGACACGAC TCCCAAGCCC CAGGGTCCTC TGCCACCAGC 1200 AGCCCCAGAG CAGTCAAGTT AGGACCCAAA CTGTGTAGAC AGAGCTACAC AAAATTAGAC 1260 AGGAGAAGCC AATGTATCCC ACTAATTTCA TAGCAAAGGT TCCTTATTAC AAATACAGCA 1320 AACCAAGGAC AGACAGCAAA GCTACTGCTC GCAGCCAAGA ACTGAAGAGT GGCTGGGAGG 1380 GAGGCACTGG GGTTCCAACA GTGGAAATCA GAACGGAGCT CATTTTCCTC CTGCAGCCCA 1440 GCCCTCAACT TCAGTCCCAT CTTAAAAATA ACCAGCCGGG GCCGGGCGCA GTGGCTCACA 1500 CCTGGAATCC CAGCACTTTG GGAGGCTGAG GCGGGCAGAT CTCTTGAGGA AAGGAGTTCG 1560 AGACCAGACT GGCCAACGTG GTAAAACCCC ATCTCTACTA AAAATACAGA AAATTAGCTG 1620 GGCATGGTAG CTCACACTTG TAATCCCAGC TACTCGGGAG GCTGAGGCAG GAGACTCACT 1680 TGAACCCAGG AGGCAGAGGT TGCAGTGAGC TGAGATTGCA CTACTGCACT CCAGCCTGGG 1740 CGACAGAGCG AGACTCCATC TCAAACAAAA AAACAAGCAA AAAAAATAAC CAGCCAGGTG 1800 CAGTGGCTCC CACCCGTAAT CCCAGCACTT TGGGAGGCTG AGATCACTGG AGTCCAGGAG 1860 CTCGAGACCA TCCTGGCCAA CGTGGCGAAA CGCTGTCTCT ACCACAAATA CAAAAATTAG 1920 CCAGGCATGG TAGCACACAC CTGTAATCCC AGCTACTCGG GAGGCAGGAG AATCACTTAA 1980 ACCCAGGAGG CAGAAGTTGC 2000
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