Tag | Content |
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EnhancerAtlas ID | HS182-11705 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:58979490-58980430 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr19:58980011-58980026 | CATGCTGAGTCACGA | - | 6 | TFAP4 | MA0691.1 | chr19:58980412-58980422 | ATCAGCTGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I058468 | chr19 | 58979821 | 58979838 |
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Enhancer Sequence | AAGGAGAATT GAAAGGAAAG CAGGTTTCCT TCAGGGGAAA GATCAAGAGT CTGGGATGTC 60 CCAGGTTGGT CATGTCACTG GACCTGACGT TGTTGGCGTC CTGGGCTGTG GACAGGGCCT 120 ATGAATTGGA CTGAGGAATG GGCAGGGACT CAGCCAGGTG TGGGCAGTTA TGGCTTGAGG 180 GTAAAGAAGA CCAGCTGGGA TGCCTGGGGC TATTGGGAAG AGCCTAGCAC CTAACTGAGG 240 AGGGGAGGGT GGCAACAGAG AGGGGAAGAA AGGGGACACC GGGTGAAAGG AGGAAGGGAT 300 TGAGTTCCTC TGTGTTCACA GGTTGTTGAG GCTGCTCCCC TGTGGCGACT GGTGAGAATC 360 ATCCAGTCCC TCAGGCTGGA TGAGCAGCCT GGAAATGTCA GGCAAGCAGG CTCAGCAGGG 420 GAGGGTCCCA GTGATGGGTA TGCCTGGGAA GCCCCTGCTG GGACTCACAG TTTCTTGCTA 480 CAAGAGCAGG AAGGGTGCAT CTGGGGAGGG TCATGAGTGG TCATGCTGAG TCACGAGTGG 540 ACACCTGGGG CTGCTCTTGG TGTGGCAGCT GAGGGCCCAG CCAGGACTTG TTCTAGCTTG 600 CTTGTGTATG GCGTTGCCAG TGGGGAGGCC AAGAAGGCAT CTGGGGTCTG GTCAGGGAGG 660 GCAGAGGGGA GGGGTCCCAG ACATGTGAGG GAAGTGCCAT CTGAAGATGG TGGGGGCAGA 720 ACCCAGGGAA GGAGGGTGAG TGTCTGAGGG ACATCATGGA AGGTGGCTGT TGGGATGGGG 780 AGCTTGGTCC TGGCTCACAG CCATACCTTA AACTAAGCTT GTCCAACCCA CTGCCCAGGA 840 TGGCTTTGAA TGCAGCCCAA AACAAGTTCG TGAACTTTCT TAAAACATGA GATGTTTATG 900 CAATTTTTAT TTTTTTTAGC TCATCAGCTG TTATTAGTGT 940
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