Tag | Content |
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EnhancerAtlas ID | HS003-18561 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr17:4622720-4623500 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr17:4623028-4623039 | AAAACAAAGAC | + | 6.14 | TFAP2C | MA0524.2 | chr17:4623088-4623100 | TGCCCTCGGGCA | + | 6.27 | TFAP2C | MA0524.2 | chr17:4623088-4623100 | TGCCCTCGGGCA | - | 6.52 | ZNF263 | MA0528.1 | chr17:4622919-4622940 | AGAGAAGGAAGGGATGGGGGG | + | 6.35 |
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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 |
GH17I004719 | chr17 | 4622738 | 4623671 |
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Enhancer Sequence | GGTGGGGCTG GGGCGGGTCC CCTGCAGGCC AGGGGCCAGA CGTCGGTTCA GTGCTCTATC 60 CTAGTGTGCC AGGGATGTAT CAGTGAACAG AAGAGACAAA AAGAACTCTT ACATTCTAGG 120 GGAGGGAGGA TAGCCAAATC TGATCAGTGG TCACTGTACA GCAGGTTTAG TGACAAGTAT 180 GAAGGAGAAA AAGCCAGGCA GAGAAGGAAG GGATGGGGGG CAGTGAGGTG CGAAGGTGAA 240 TTCGGAGTAA GGACCCAGCG GAAGTAAGCA ATGTGGGTGA GCAGGAAAGG AGGGTTCTGG 300 GCAGAGAGAA AACAAAGACT CAGAGGTGGG GCAGCCTGGG GTGTTGGAGG AATGGGGAGG 360 TGCCATCGTG CCCTCGGGCA GGAGCAGCCC TGGAGGTCCC CAGCTTCACA AAGGGCTGGA 420 TTTCACCTCT CCGGATGCCT TTGTTCAGGG TTCTCACTGC ACAGCCACAC ACAGCAGGCC 480 CGGAGGGCAA CTTAGGGAGA AGAACTAAGT ACCAGGAGAG GAGGAGGAGG TGAGGTCAGG 540 GGCTAATGGA GAGCCAGACG GTGCAAGGCT GTTAGCGGAG AAGGACGTCA GCTTTTCCTG 600 GAGAGGAGCC AAGGAGGCTC TGAGCAGGGA GTGCAGTGCG CACTGTACCA TAACCGCACG 660 GCCTGGGCTG CTGGGGCCCT GGGGGCCTGT GCGAGTTTGT GGTCCTGCCC AGAGTCCCCG 720 TGGGAACCCC ACGGTGGGCC AGGTGACAGG GTGATAGGCC CTGGTCTGAC TCCAACACCC 780
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