Tag | Content |
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EnhancerAtlas ID | HS012-15394 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr19:8749330-8750700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr19:8749595-8749610 | TGAACTCTTGCCCTC | - | 6 | SCRT1 | MA0743.1 | chr19:8749863-8749878 | ACACACTTGTTGCAT | - | 6.01 | TCF7L2 | MA0523.1 | chr19:8749983-8749997 | TGCCTTTGATGTCA | - | 6.22 |
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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 |
GH19I008637 | chr19 | 8747255 | 8750711 |
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Enhancer Sequence | TTGTGAAAGA ATCTCTCTAA CACTATTTAA AAAACCCTGC TGGGTGTTTA AAAGCCCTAC 60 TGGGGTTGCC ATGTTTTGGC TGGGTCCCGG CTCTTTTGTA TAACAGATGT TACCCAGATG 120 TCAGCTGGGG TCAATAGAGC CTCAGAGATT TGGCGTCTGC CTCTCTCCCA CGACCTGTGG 180 GAAGCCTGGT GCCCTCTGTG AGATGCTTGT GAATTCCCAG GGCCTCTGTT CTCATGGTTG 240 CGTCTTGGCC TGAGTTCCTG CCCGCTGAAC TCTTGCCCTC ACCCACCTTC CTGGGGCCAG 300 TGCTTTGCAG GTGAACCGGT CCTGTGTTCT TGATTTTCCC CCAGATCACT CTTGCACATG 360 GACTGCCTGC AGGTTGCCTC TCAAGATACT GTGCTCTCCC AGTCTGGCCA ATGTAGCAAG 420 AACCTATTGT TCCTGCTGTA GTTTTTTTTT TTTTTTTTTT TTTTTTACCA TTGCTTGAGC 480 TTCTGCATAA GATGTTGCTT GACAAAGCAT TCCACCACCA ACAGGAAAAG TTTACACACT 540 TGTTGCATAA CACAGCATAG AGCGTGATGA CCGGCTTGGA GTTTACCAGG CTGTCCTGTG 600 AAGGGGAAGT TCACTTAGGA CACCCGGGGC CAATGGCTGT GAGCAGCAGA AGGTGCCTTT 660 GATGTCAAGC TGTCTTGAAC GCTGCTGCTC CCGGGTGGGT AAGAGCTGGC ACAGTCCAGA 720 AAAATTGAGG CGGCGACACG ATGAGAGACA GCAACCCATC CCCAGACAAA CCTCAAGAGA 780 CCAGAAGCAG CCACATTGCA CCAGACTTCT GGAAAATTAG GCAAGCGTTG GCAACAGAAT 840 ATGTTGTGGA CTCTTCTCAC AGTTTCTGTA ATCATTAACT GCTTTCTCAG GGTGTGGATA 900 TTCAAGGACC AGAGGTCAAA GTTACAGCAA CAGCACCTTG CAAGGGGCAG GGGTGAGGAG 960 AACCTCCTTG GGCAGGTCGT GCTGTATGGG ATAAGCCCAG AACTGGTTTA GTTCTGAGAC 1020 GAGGGTGCAG ATAGTATTGG AAAGATGCAT ATCACTCAAG CCTGGAAGAA GACCAGGGTT 1080 ACACTTAACC TTGACTGCAG TTCAATGCCT CGGTAATATG GACTGAATTG TAACTAAGAC 1140 TGTTCTCTGC AAGGTTTGCT TGGTTTCTGC ATCTTTGTAA TTGTAGCATT TGGTGTTCAC 1200 TTGAAGGATG GGTCTTCAAG AGCATATTCT CCAATGTTTC TTTCTCACGG CTCACCACAA 1260 CCTCGACCTC CCAGGCTCAA GTGATCCTCA CACCTCAGCC TCCCGCGTAG CTGGGACTAC 1320 TGGCATGCAC CACCACACCT GACTAATGTT TGTTTTTTTT TTGTAGAGAT 1370
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