Tag | Content |
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EnhancerAtlas ID | HS062-07110 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr17:45078280-45079520 |
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) |
CTCF | MA0139.1 | chr17:45078668-45078687 | TGCTGTCCTCTAGTGGCCA | - | 6.89 | ETV6 | MA0645.1 | chr17:45078720-45078730 | AGCGGAAGTG | + | 6.02 | SPI1 | MA0080.4 | chr17:45078716-45078730 | AAAAAGCGGAAGTG | + | 7.73 | SPIB | MA0081.2 | chr17:45078718-45078730 | AAAGCGGAAGTG | + | 6.92 | SPIC | MA0687.1 | chr17:45078716-45078730 | AAAAAGCGGAAGTG | + | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 45078799 | 45079000 | chr17 | 45078376 | 45079065 |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I047002 | chr17 | 45078367 | 45078967 | GH17I047001 | chr17 | 45079167 | 45079366 |
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Enhancer Sequence | ATCATGAGGT CAGGAGTTTG AGACCAGCCA GACCAATGTG GTAAAACCCC GTCTCTACTA 60 AAAATACAAA AATTAGCCGG GCGGGGTGGT GGGCACCTGT CATCCCAGTT ACTTGGGAGA 120 CTGAGGCAGA AGAACCGCTT GAACCTAGGA GGTGGAGGTT GCAGTGAGCC GAGATGGTGC 180 CACAGAACTC CAGTCTGGGC GACCTTCCTG CACTCCCGGT GTTCGGGGAC CAACAAGGCG 240 TAATAAGGAG CCAGAGACCA AGGCCCAAGT CTCAGCTCTA ACTGAGTATT ATGGGGGTAT 300 TAATGTCCAC CTCCCAGGAT AGGGAGCACA GAGCAAGGAA TACTAAGTAT TGAAGCCCTG 360 AAACGCCCAC TTCCTGTACC TGAGTCGCTG CTGTCCTCTA GTGGCCACTG GATAAATTGC 420 ACAGCACGCC GGCCTGAAAA AGCGGAAGTG AGAGATGCTT TTCCCCACTT CTGAATCTAC 480 CAGATGCTGG GGGGTTCTCA ACCATGCTCC ACTCATGACT TCCTTTTTAT AAAATGTATT 540 TTGTGTAATT ACAGTAATTT TTGAACATTT TAGGCAGATT TATTGAGGTA TTGACATATA 600 ATAAACTGCC TAGAGATTAC AATTTGATAA TATCTGAGCC TTAGTATACA GCTGAAATCA 660 TTATCACAAT CAAGATAGTG AAGAAAGCCA TCCTCCCAAA AAATTTCCTT GTTGCCCCTT 720 GGTGATCCTG CTTCCTGCCC TTTCTACTTC CCTCTCACCC CCAAGCAACT ACTGATCTGC 780 TTTCTTTCTC TTCTCTTTTT TCCTTTTTTT TTTTTTTTTT TTTTTTGAGA TGGAGTTTCA 840 CTCTGTCACC AGGCCGGAGT GCAGTGGTGA GATCTCGGCT CACTGCAACC TCCGCCTCCC 900 AGGTTCAACA GATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGACTACAG GCACCTGCCA 960 CCACGCCCAG CTAATTTGTG TATTTTTAGT ACAAATGTTG TATTTGTATT TGTATTTAGT 1020 ACAAATGTTG GCCAGGCTGG TCTTGAACTC CTCGCCTCAA GTGATCCGCC CACCTCGGCC 1080 CCCCAAAGTG CTGGGATTAC GGGTGTGAGC CACCACGCCT GGTCCTGATC TGCTTTCTGT 1140 CATCATAGGT TAGTTTATAT TTTCTAGTGC TTTCTAGACA CGGAATCATA CAGTGTGTAT 1200 TTTTTTGGTC AGGTTTCTTT CACTCACCAT AATTATTTTG 1240
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