Tag | Content |
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EnhancerAtlas ID | HS108-17196 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:46697300-46698510 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Spz1 | MA0111.1 | chr17:46697907-46697918 | GCTGCTACCCT | - | 6.02 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_39949 | chr17:46697189-46698555 | K562 | SE_47101 | chr17:46628526-46699689 | Panc1 | SE_56734 | chr17:46685753-46705899 | VACO_400 | SE_56820 | chr17:46685753-46705899 | VACO_400 | SE_57368 | chr17:46696158-46701540 | VACO_503 | SE_58204 | chr17:46693138-46711614 | VACO_9m | SE_68498 | chr17:46671549-46704938 | TC71 | SE_68499 | chr17:46671549-46704938 | TC71 | SE_68500 | chr17:46671549-46704938 | TC71 | SE_68501 | chr17:46671549-46704938 | TC71 | SE_68502 | chr17:46671549-46704938 | TC71 | SE_68503 | chr17:46671549-46704938 | TC71 |
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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 |
GH17I048618 | chr17 | 46696232 | 46697530 | GH17I048620 | chr17 | 46697956 | 46698411 |
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Enhancer Sequence | AGCACCGGCT GGGCCTGGGT AGCCCAGGAT GGGGCAGGAG CCTGGTCTAC ACCAGCTGTA 60 AAGCCAGATT CATTTTGCAT CCCTAATGAA ACCCTCTTTG GAGGGTGCCT GTCCGGGCCT 120 GCCTGATGCG GAGCTCCGCT TTCTCCTGCC TCCCGCCGTC TCTTGGATCA GTTCGTCCTT 180 TCGTTGGAGG AGGGTAGGCC TGGCCTTTTC ACTTGCAGTC TCCCTTCATT CGGGCCATGC 240 TTCGTTCCCA ACTCTACCCC AACTCGCAGG GTCTCCGCGG GCCGCAGTGT TGCCGGCTTG 300 GGTTGGGGAG AGGCTCCTGA GGTAGGCGGG CTCGGGAGCG CCGGCCCGCC GAAGCGGAAT 360 CCCAAGGCCT GGATGAGAAG CGCAGGCTGC CGAGAACTGC GATCTTCATA AGAGGCTCTG 420 GCGAAATCCC TCAGTCTGAG AGGGACAAAA ATGTGCCTCT TGAAACTGAG TTTAATTCTG 480 GGGTCCTTTT GGGAGGTGAA TTTTTCTACT GAGACATTTC TGCTTCACAC TCAATGACCT 540 CTCCACCCTT TGCAGAGGTG CTTACCCAGG GCTCAGCCCC TACCAACCCA GCCCACCTCA 600 GACCAAGGCT GCTACCCTGT GGCTCAAACT GGAGCCTCCA ACCCCAGGTG GGGGCCGAGA 660 ACCCTAAGGC GTTGGCTCCC TTTGAATGGA AGGAAAGAGA TTCCAGCCCT CTGGAGGCCT 720 CTGTCTAGAC CTAGGCACCC TACTGCAGGG AAGAACAGAG GGAAATTACT GTGTTCCTCC 780 CTTGCATCAT ATTTTAAAGC GGCCAAACTA AGGTGACATT CTCAGTGGCT GAGGGAGGAG 840 AGCTACCCCC AGGAGGTGCA GGAAGACCTA CCTTCCCTCC TATTCTCTAG TCAATGAGGA 900 GGTTTCAGGA CCTCATTGCT CCCCAGACCC TGTGCCCTCT CCAAACAACC CACATTTCCT 960 TCCCTCCCCG CTCGTTTTCC AGTTCTCCTG TTGGAAGGCT CTTGATCAGT TTAACCAGTA 1020 GTCTTGGGAC CTGGGGTCTG GGACTGGCTC TCAGCTCCAC CTCTAGAGAG CTCTGCAGGG 1080 GACCTTGCCC TGCAGGGTGT AAGGAGAAAC CTCCTGGACT CAGCAATCTT TTTTTTTCCA 1140 AGCCTTTCTC CCGACAACTG GGATCTCTAC CTATGGTCAG GCCCAGAGAG CCAACACAGA 1200 ATAAGACACA 1210
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