Tag | Content |
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EnhancerAtlas ID | HS060-18042 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:45225220-45226350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr19:45225788-45225802 | CAAAAGGGGAAGTG | + | 6.41 | SPIB | MA0081.2 | chr19:45225790-45225802 | AAAGGGGAAGTG | + | 6.07 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09606 | chr19:45225026-45227473 | CD14 | SE_23877 | chr19:45225227-45225635 | Colon_Crypt_2 | SE_31568 | chr19:45225186-45226205 | Gastric | SE_34750 | chr19:45225301-45226193 | HeLa | SE_53360 | chr19:45224892-45226462 | Spleen | SE_62704 | chr19:45221152-45271677 | Tonsil | SE_65330 | chr19:45224918-45226537 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 45225441 | 45225906 | chr19 | 45225274 | 45226089 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I044721 | chr19 | 45225041 | 45229949 |
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Enhancer Sequence | TGCTAGGATT GCAGGTGTGA GCCATCATGC CCGGCCCTGA TTCAGGTTCT AACAGGATCC 60 CTCTGGCCAT GAGGTGGAAA GAGACTGTTG GGGGCAGAAT TGTAAAGCGA GGGACAAGAA 120 GAGTCAGGGG TCTCCAAGCT TTGAGCCTGA GCCACTGCAA GGATGAAGCT GCCATTTCTG 180 AGGCCAGAAG GCTGCAGGCA GGGCTGGGTT GGAGATTGGA ATGAAGATAG GTCTTGTTTG 240 AGGCCAATGA GGAGGGAGCC TCACCCGAGG CACACAGGCT CCAGGCGGGA AGTTGGCGAC 300 AAGTTGTGGA CTGTGGTTTT CACCCACCTC ATGGGGCCCC CTCATCCTCT CCCCCAACTT 360 CCCCTCACGC CGTGGTGGAG CCAGCTTTGT TTGTTTCCCC CCCATCATCC GTTTCATGAT 420 GGGGAAGACT GGTTTTCCCC TAACCCAACA GACACCTCTT CCCTCAGCCT GTCCCTGACC 480 CTCCCACCTC GGGAAGCCCC GAGCGGGCCT CCCAGAATGT CCCGGCAGGA AGGGGCTGCT 540 GCTACCGTTC ATCCAGCCAG ATGAACCCCA AAAGGGGAAG TGGGTCACCC GTAGTCACCC 600 GGCTCATGGT CAGCTCGGGA CTTCAGGATC TCGTCTCTTC ACTGCACCCA CCACAGCCCT 660 GGGAGGTTTT CCATGCACGC TTCTCATTCT CCCCACATTT CACACGAGAA AACAGGGGCT 720 CCAAGAGAGG CCCACACTCA CCTAAGGAGC TCGAAAGATA GGGGCATCTG GATTTGAACC 780 CAGGTCCTAG CAGATGTTGT TAGCTCAGAG GAGAAGGCAG AGAGGGTGAA CAGAACCCAG 840 CCTGCCCTCC CAGATCCAGT GGGAAGGCAG ACTTGTCCCC AGGTAATAAT AGCCCAGCAG 900 TGTTCACAGC CTGGGATGGA GGAGCCCAGG AGGCTGCAGG AGCTCAGAGC GCATGCCTGA 960 CCCAGCCTGG GGTCAAGGAG GGCTTCCTGG AGGAAGGGAC AGCTCATCTG ATACCTAGAG 1020 GATGAGTGGG AGTTACTAGG TGTAAATAGT GCAGGGAGAG GGAAGAGTAT GTGCAAAAGC 1080 CTAGGGTTGA GAGGAAACCT AGGGGCTCCA GCAAGGCGCA GTGGCTCATG 1130
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