Tag | Content |
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EnhancerAtlas ID | HS145-11541 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr19:12404310-12405500 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr19:12404654-12404674 | CCACACACAAACCCCACACA | + | 6.06 | RREB1 | MA0073.1 | chr19:12405060-12405080 | CCACATCCCAACCACCCCCG | + | 6.21 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGTGGTTAT TCTCTTCTTC CTCACATGTG AAATGTTAAG GAAAACAAAA TAAATCTGTT 60 TAAAAAGAGC CATACATTGC TATCTGAAAA CAAACGACAA AATTCTGTGT CTATTTGAAA 120 TATCGTCTTG CTGACAAAGG GTTCATAACG TTACTGGGAA TTGAGGAGTG AAGTTAGCAT 180 ATGGAAGGCT CTGGAAACCA AAAGATTTAC TGTTAGCCCC AAGAGGAGTT AGGATGAAGG 240 GACAGGTCTC AAAGACCCTG ATGCCAATAT CTTTGAAAGC CTCGGAGGAG AAATGGTCGC 300 CCTTGGAAAG AAAGGACTGA AGAGCACAGA GACCACAGCT CCTCCCACAC ACAAACCCCA 360 CACACGAGTC TGGTTTGTGC CTAGTGACCC TCCCACCGTC ACCGTGCAGC CTCCTCACCG 420 GGCTCACAGG AACTGCGAGC CAGGCTGGAG GCGAGATTGC AGTTAGATAT TAACCAGGTG 480 CCCTCAGCCC CGCTGCTTCA CAGGAAGCCG CCTCCCTGAG AGTCAGGTCA CAGCAGACGC 540 TGACCGCCGG CTTCCCCATT GGCCTGGGGA TAAGATCTCT GAGAGTTGCT CAAGAGTCGT 600 CTAAGTTCTT TCTCAGATCT TGAATTCCAG CGGAAAGGCT GGCGCCAAGC AGGCTGAAGA 660 CCCCACAAGG AAGCCCACTC AGCAGCAGAA TGCGGTTTCT TCACCTCCAG TCCCAAGATT 720 CACCCCTCAC TTCTCCACCA ACCAGCGACC CCACATCCCA ACCACCCCCG TCCAGACCCC 780 TAAACACCCC ATCCTCAAAC CTCTCACGGA GGCGGATCTA GGGTGTCCTC TCCTATTAAA 840 CCGTTTCTGC TGCAGCCCTC GGCGTCCGGG TGCAGTGACT TGGGCTGCGA ACCTGTACTG 900 GTTCCGCCGC ACAATCTGGG GAGAAGCGGG GCTGAGGGCG CGGAGCTGCC CAGAGAGGGG 960 CGCCGGGGCC GGGGCCGCAG TCGCAGCTCA GGGACGGGAC AGGACGCCCG GGGTCCCGGC 1020 TGCCGGCCCA GCCCCACCCT GCGGCCAAAC GGACCGAGGA CCGAGGTGCG CAGGGGGCGC 1080 TCAGGTCCCA GACCCCAAAG ACGCTGCGGC GAGGCCCGGG TCCCGCCACA GCCGGTTCCG 1140 ACTGGTTCCG ACCAGCCCTT CGCCCTGCCT CAGGACGCCG GGCCCCGCAC 1190
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