Tag | Content |
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EnhancerAtlas ID | HS073-07777 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:45225020-45226240 |
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 | CACTCAGCTC ACTGTAACCT CTGCCTCCGG GGTTCAAGTG ATTCTCCTAC CTCAGCCTCC 60 TGAGTAGCTG GGATTACAGG CATGCACTAC CACGCCAAGC TAATTTTTGT ATTTTTAGTA 120 GAGACGGGGT TTTGCCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCA 180 CCTGCCTCAG CCTCCCAAAG TGCTAGGATT GCAGGTGTGA GCCATCATGC CCGGCCCTGA 240 TTCAGGTTCT AACAGGATCC CTCTGGCCAT GAGGTGGAAA GAGACTGTTG GGGGCAGAAT 300 TGTAAAGCGA GGGACAAGAA GAGTCAGGGG TCTCCAAGCT TTGAGCCTGA GCCACTGCAA 360 GGATGAAGCT GCCATTTCTG AGGCCAGAAG GCTGCAGGCA GGGCTGGGTT GGAGATTGGA 420 ATGAAGATAG GTCTTGTTTG AGGCCAATGA GGAGGGAGCC TCACCCGAGG CACACAGGCT 480 CCAGGCGGGA AGTTGGCGAC AAGTTGTGGA CTGTGGTTTT CACCCACCTC ATGGGGCCCC 540 CTCATCCTCT CCCCCAACTT CCCCTCACGC CGTGGTGGAG CCAGCTTTGT TTGTTTCCCC 600 CCCATCATCC GTTTCATGAT GGGGAAGACT GGTTTTCCCC TAACCCAACA GACACCTCTT 660 CCCTCAGCCT GTCCCTGACC CTCCCACCTC GGGAAGCCCC GAGCGGGCCT CCCAGAATGT 720 CCCGGCAGGA AGGGGCTGCT GCTACCGTTC ATCCAGCCAG ATGAACCCCA AAAGGGGAAG 780 TGGGTCACCC GTAGTCACCC GGCTCATGGT CAGCTCGGGA CTTCAGGATC TCGTCTCTTC 840 ACTGCACCCA CCACAGCCCT GGGAGGTTTT CCATGCACGC TTCTCATTCT CCCCACATTT 900 CACACGAGAA AACAGGGGCT CCAAGAGAGG CCCACACTCA CCTAAGGAGC TCGAAAGATA 960 GGGGCATCTG GATTTGAACC CAGGTCCTAG CAGATGTTGT TAGCTCAGAG GAGAAGGCAG 1020 AGAGGGTGAA CAGAACCCAG CCTGCCCTCC CAGATCCAGT GGGAAGGCAG ACTTGTCCCC 1080 AGGTAATAAT AGCCCAGCAG TGTTCACAGC CTGGGATGGA GGAGCCCAGG AGGCTGCAGG 1140 AGCTCAGAGC GCATGCCTGA CCCAGCCTGG GGTCAAGGAG GGCTTCCTGG AGGAAGGGAC 1200 AGCTCATCTG ATACCTAGAG 1220
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