Tag | Content |
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EnhancerAtlas ID | HS012-09516 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:53134640-53135970 |
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) |
HOXA13 | MA0650.2 | chr12:53135128-53135139 | GTTTTATGGGG | - | 6.02 | REST | MA0138.2 | chr12:53135343-53135364 | TTCAGCACCAAGGACAGAGCA | + | 9.11 | SP2 | MA0516.2 | chr12:53135821-53135838 | AGAAGCCCCGCCCTCCT | + | 6.03 |
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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 |
GH12I052741 | chr12 | 53135281 | 53135430 |
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Enhancer Sequence | ACAGTTGCTT TCCTTAAAGA ATTTAGAATA GAGTTGCTAA TCAAAATTTG TGTAAGTATA 60 GTACAATATC AGTATGAACA TCTTTTGTCT TATAAAGTGT TTTTTACATA TATTACTTCA 120 TGTGTTCTTC AACACATCCC AGAGAGGAAG ATATTCTTTT TATTACCACA TTAATGAATA 180 ATAATACTTA ATGTTTTAAA TCATTCTCCT CCTCTGGAAG TGTCCAGTTT CTAATGTGGC 240 TCAGCATGAA CCTAGCCTCA ATCAAGAGAA GACTAGCTTC TTAGACTTTT TTATTTTTAT 300 ATCCCTGTCA TCACAATAAT GAGGGAGTTA ACTTAAAATA ACAATCCATG TTAAAATAGG 360 AAGAAAATAT AATACTCTAA TCACCAATGA CAAATACTTT CCAGCAGCAG GAGGCAGAAA 420 GGAAAACATG CCAATATTCA TACGTTTTAT TATTCATAAA GACTTAGAGG CAAATTATTT 480 TGGTCTTGGT TTTATGGGGA ATATAACAAA ATAGACAAAG TCTGAGACTA TTTTAAAGTC 540 GGGCTCTGGA CCAAATATTT ACCTGATCTT AGACAGAAAA TTTGTATGCC CAAATGCAAA 600 TCGTCAGAGC TGAAGCAGGG AATGGGGAGA GTTGAGTTTG GAGGAAGTGA CTACAGTGTC 660 AGCCTCCTGA AATAGAAAAG GCCACCGGAT ACCTGGGCCA GATTTCAGCA CCAAGGACAG 720 AGCACCGCTT CCTGGACGGC GTCTAAAGAC TCAAAGGCCT CTCACTAAAG TAACGCTGTG 780 CCGTTGAAGA CCAGAAACAC ACCCCACACA CACACACACT GTCTTGAAGA AACAAAACTA 840 CACCTATGTT ATTAATATAG CGTGGGAGTG ACAAGCATGG ACTCCGGGGC TCAATTGCCT 900 ATGTTCACAC ACTGGCTCTA CCACTTGCTA ACTGTAACCT GTGACACAAT GTGACCTTCA 960 CGTCTCTATA CCTCCTTTTC CACATCTGCA AAATAAGGAT AATCATACCC ACCTCATAGT 1020 GATGGCAGCG GCTGCAGCAG GGAGGCACAG CTAGGGCTGC ACACTCCATG GAGCCAGTGG 1080 GAGCCCCACC TCTTCTGAGT TGGGGCGGGA CCTCCCCAGG TGATGCTGCA GCCATCCAAA 1140 TTGCAGCTGC AGACCCAGTC CTCCTGTTCT AAGGAGAAAG CAGAAGCCCC GCCCTCCTCG 1200 TCAGGGCTAC AGCCCCCCAA AATGTGGCTG TGGATCGGAG CCTCCCTGTG CTCTTTAGAG 1260 GTCCAGGAGT AGGCAGGGTC TGCCTTCCTG GGTGCAGCAG CAGCTGCCTG ATCTACAGCA 1320 GCAGACCTGG 1330
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