Tag | Content |
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EnhancerAtlas ID | HS034-14967 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr19:18451530-18452540 |
Target genes | Number: 25 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr19:18452266-18452283 | GGGGTCATTTTGACCTG | - | 6.51 | RREB1 | MA0073.1 | chr19:18452164-18452184 | CTCCCCCCCACCCCCAAACC | + | 6.01 | ZEB1 | MA0103.3 | chr19:18452039-18452050 | GGGCAGGTGGG | - | 6.14 |
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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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Enhancer Sequence | CTGGCTGATG GGGGCTGTAG CGGCAGCGGC CGGGGGCAGA GGCGGGGGCG GCTCCGGGAC 60 TGCGGGGCCG AGAGGGGCAG GTGCTGGAAG TCCTCTCAGA TTTGGAAGGT GTCATCACCC 120 GCGGGAGCCC CGCGCAGCCC AGGCTTCCTG GAAAGTGGAG GAGGAGGAGC CTTGGGGGTC 180 CCAGGGTCGG GAGTCAGGGC AGTCGGGCGC GGGGCTTGGG GGGCCGGGCA AAAGCCCGGC 240 GCTGCGCAGG CCCCCCTGGC GTCCTTTCCT CCCAAGGTGG GGATGGTGAC CCTCCTGGCA 300 CCTGCCTCCT CTGTCTGGCC TGCGGGCTGG ACTGGACCCT TCCTCCCTGC CCCTTCCGAG 360 GTCCAGCCTG TCCCCACACC GCTCCCCCAA CCCCTGGCCC CAGGGGACAA AGGCCGATTT 420 GCGGGCAGGA AGTGTCCCAG TGACAAATGA ACCTCCCAGT CACTGCTCGC CGCGCCCTGC 480 GCTCCTGGGG GGCTACTCTC CCAAGGCAGG GGCAGGTGGG GGTCCGGGGA CCTCGGGCTC 540 TCCCAGCTGT CCCAGGGACT GTCTTCAGCG GAAACCTTTT TGTGTTTTGT GCCAGGGCTG 600 TTTGTTGGTG AGTCAGGGCC CCTGCTGTCA CCGACTCCCC CCCACCCCCA AACCAACTGT 660 TTCTCCTCCC TGAGACTCCG CCTCGGGGCC ACGTGGGGCG CCAACTTCCG CTGGGGCCTC 720 AGAGTCAAGG AGTGGGGGGG TCATTTTGAC CTGCTGTCTG GAGGGGTCAG AGTGGGAAAT 780 CCAGCAAAGG TGCACACAGG TGTTTTGTGG CTGTTGAAGG GAGATTGAGG CTGATCCAGG 840 AGATTCAGGG AAGAAGGAAG AAACAAGGCA CCTGCTTAAC AGGTGTGTAT AATTGGGAGG 900 AGGGTCACTG CCCCCATCCC TTCCAGCCTT CCTTTATCTG GTTATTTATT CCAGCACTTT 960 TTGCATGAGC TGATTACATC TTTACTGTCT CCATTTTGCA GAAAGGGAAA 1010
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