Tag | Content |
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EnhancerAtlas ID | HS182-11467 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:45225160-45226350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:45225175-45225190 | TGAACTCCTGACCTC | - | 6.22 | 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 | TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCA CCTGCCTCAG CCTCCCAAAG 60 TGCTAGGATT GCAGGTGTGA GCCATCATGC CCGGCCCTGA TTCAGGTTCT AACAGGATCC 120 CTCTGGCCAT GAGGTGGAAA GAGACTGTTG GGGGCAGAAT TGTAAAGCGA GGGACAAGAA 180 GAGTCAGGGG TCTCCAAGCT TTGAGCCTGA GCCACTGCAA GGATGAAGCT GCCATTTCTG 240 AGGCCAGAAG GCTGCAGGCA GGGCTGGGTT GGAGATTGGA ATGAAGATAG GTCTTGTTTG 300 AGGCCAATGA GGAGGGAGCC TCACCCGAGG CACACAGGCT CCAGGCGGGA AGTTGGCGAC 360 AAGTTGTGGA CTGTGGTTTT CACCCACCTC ATGGGGCCCC CTCATCCTCT CCCCCAACTT 420 CCCCTCACGC CGTGGTGGAG CCAGCTTTGT TTGTTTCCCC CCCATCATCC GTTTCATGAT 480 GGGGAAGACT GGTTTTCCCC TAACCCAACA GACACCTCTT CCCTCAGCCT GTCCCTGACC 540 CTCCCACCTC GGGAAGCCCC GAGCGGGCCT CCCAGAATGT CCCGGCAGGA AGGGGCTGCT 600 GCTACCGTTC ATCCAGCCAG ATGAACCCCA AAAGGGGAAG TGGGTCACCC GTAGTCACCC 660 GGCTCATGGT CAGCTCGGGA CTTCAGGATC TCGTCTCTTC ACTGCACCCA CCACAGCCCT 720 GGGAGGTTTT CCATGCACGC TTCTCATTCT CCCCACATTT CACACGAGAA AACAGGGGCT 780 CCAAGAGAGG CCCACACTCA CCTAAGGAGC TCGAAAGATA GGGGCATCTG GATTTGAACC 840 CAGGTCCTAG CAGATGTTGT TAGCTCAGAG GAGAAGGCAG AGAGGGTGAA CAGAACCCAG 900 CCTGCCCTCC CAGATCCAGT GGGAAGGCAG ACTTGTCCCC AGGTAATAAT AGCCCAGCAG 960 TGTTCACAGC CTGGGATGGA GGAGCCCAGG AGGCTGCAGG AGCTCAGAGC GCATGCCTGA 1020 CCCAGCCTGG GGTCAAGGAG GGCTTCCTGG AGGAAGGGAC AGCTCATCTG ATACCTAGAG 1080 GATGAGTGGG AGTTACTAGG TGTAAATAGT GCAGGGAGAG GGAAGAGTAT GTGCAAAAGC 1140 CTAGGGTTGA GAGGAAACCT AGGGGCTCCA GCAAGGCGCA GTGGCTCATG 1190
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