Tag | Content |
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EnhancerAtlas ID | HS012-04918 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr11:83275570-83276780 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mecom | MA0029.1 | chr11:83276145-83276159 | ATGATAAGATAATT | + | 6.05 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 83275760 | 83276175 | chr11 | 83276215 | 83276362 |
| Enhancer Sequence | TTCTGCTGCT TTGGCAGGTA ACATATGGGG ATGCAAAGGA AAAAATTCTG GCATCTATGT 60 TTTTGGGGTT TACTGAGGGA TCTAACCCTC CATCCACTGA TAAAATTCTT TTAAGAAAGT 120 TACATGAGTG AATGATTGTT TGCATTTATT ATTGGTGGGT TATCTACTTG TTTAGAGAAG 180 ATTGATAATC TTGCAACAAG GATTAAATAA AACCATTCCA TCTCTCATAA TGTCTTATAA 240 TGCCTCCCCA TTCGTCATCA TCATGATCAT TATGCTGGTC AAGACAAAAA GTTAATCAGC 300 CACAAACAAA CATAAGAAGA ATTTCTTTTT TTTTCTGCAC TGATTGGATC AAGGAAGGGG 360 ATTTGCAAAT ATCTTCTAGT CAAAGAACTT CATTCCAAGT TGCCATTGCA CTTTATGCAT 420 TACCTAATCC AAACAGTTTA CATAACTGTA TTATAATCAA TCATGCAGTT CTTTATCTGT 480 TTCCCTCACT GGACTATGAT CTCCTTGAGG GCAGGCGCCT ATCTTAATGA CTATCATGTT 540 GCCATTCACT AGCATAGTTC CTGGTACAAT CCCTCATGAT AAGATAATTG TATTTCTATA 600 ATTTGACTTT AAGACTACAA ATCCAAAGGC CACCTCAGTA CTCTGTTACT GAGTACTGAG 660 ATTATAATAT GACCATTGTG CTGGAGAATC AGTTCCAACT GCAATCTGAA GCTCCCAGAA 720 GGGTGGATAT CTGCATCCTT AACTCACATC TCAAACTGTT CACTCAGCAA ACAAAGCAAA 780 AACAATATAT CTTCTCTTCT TCCTACTTCA CTACCTTTAG AGTTATGTAA AACACTTTAA 840 TTTGCACCAG AACACTGGGG AAAGAGAAAA AGGCAGCCAG GATAATATAA CAGTATCTTT 900 ATTAAGCCCT TGTGCAGTTT TAAAACGTCA GTAACTTGAA TTGAGAACAT GGTAGAGGCA 960 ACTTACAAAT CATATTTGAA AGCAAACTGA ATTTTCTCAG AACTGCCAGA AATTTCTATT 1020 CAGTGCAGAG TACACAGTGA AATTTTTCCC AGAGTATGTC TTGTCAAATA ATTATTTAAA 1080 TGTTGGATTA ATCACTGTTG AATTGGTTTG TTTTCTACAG GGCCATCAGA GATTTCAATG 1140 CACTGTCAAT CTACAAGAAG GGTATATGAT ATGCAGTTGT TTCACAAACA CTGTAACAAA 1200 TGATTTTGAA 1210
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