Tag | Content |
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EnhancerAtlas ID | HS047-17688 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:45225230-45225940 |
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: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I044721 | chr19 | 45225041 | 45229949 |
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Enhancer Sequence | GCAGGTGTGA GCCATCATGC CCGGCCCTGA TTCAGGTTCT AACAGGATCC CTCTGGCCAT 60 GAGGTGGAAA GAGACTGTTG GGGGCAGAAT TGTAAAGCGA GGGACAAGAA GAGTCAGGGG 120 TCTCCAAGCT TTGAGCCTGA GCCACTGCAA GGATGAAGCT GCCATTTCTG AGGCCAGAAG 180 GCTGCAGGCA GGGCTGGGTT GGAGATTGGA ATGAAGATAG GTCTTGTTTG AGGCCAATGA 240 GGAGGGAGCC TCACCCGAGG CACACAGGCT CCAGGCGGGA AGTTGGCGAC AAGTTGTGGA 300 CTGTGGTTTT CACCCACCTC ATGGGGCCCC CTCATCCTCT CCCCCAACTT CCCCTCACGC 360 CGTGGTGGAG CCAGCTTTGT TTGTTTCCCC CCCATCATCC GTTTCATGAT GGGGAAGACT 420 GGTTTTCCCC TAACCCAACA GACACCTCTT CCCTCAGCCT GTCCCTGACC CTCCCACCTC 480 GGGAAGCCCC GAGCGGGCCT CCCAGAATGT CCCGGCAGGA AGGGGCTGCT GCTACCGTTC 540 ATCCAGCCAG ATGAACCCCA AAAGGGGAAG TGGGTCACCC GTAGTCACCC GGCTCATGGT 600 CAGCTCGGGA CTTCAGGATC TCGTCTCTTC ACTGCACCCA CCACAGCCCT GGGAGGTTTT 660 CCATGCACGC TTCTCATTCT CCCCACATTT CACACGAGAA AACAGGGGCT 710
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