Tag | Content |
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EnhancerAtlas ID | HS012-06902 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:126372080-126373710 |
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) |
ZNF263 | MA0528.1 | chr11:126373669-126373690 | CTCTTTCCCTCCCTCTCCTTC | - | 6.48 | ZNF263 | MA0528.1 | chr11:126373672-126373693 | TTTCCCTCCCTCTCCTTCTCT | - | 6.54 | ZNF263 | MA0528.1 | chr11:126373663-126373684 | CTCTCCCTCTTTCCCTCCCTC | - | 6.79 |
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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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Enhancer Sequence | CCATTCAAAA GTTCTCTGCC CACTTGAAAA GGGTCTCACC TTGGGCAGAT CTCATGCTGC 60 CTAGCACAGG GGATGCATCC ACTCACCGCA CTGGACCAGC ACACCAGCTA GGGAAGCACA 120 GTTTGAGAGC TCCTGGGACC TGTCCTGGCT GTGCTGCCCA CAGCCCCTCC TCCACTCCTC 180 CTGGCAAGAG GAAACAGGAC AGCTCCTCCT GCCCAGGCAC AGTCAGAAGA AGCTGTCCCT 240 TCTGGGCAGG CACACCTCAG AGGGAAAGCA ATTCAATTAA GCCCTGGTTC ACAGCGAGTG 300 CTAAAAACCT CCCTCTGGAG AACCATTTTC TGCTATAGAT TTTTAAGACC AGCAGCTGGA 360 GAATCACTCT TCCTTTTTCT CTTTTGGTGC TGTGTCTCTC TAGTCAATAA ATAAGTGGGA 420 AATAAAGTAT TTGCAAGAAA ATAGAATGCA GTCGAAAGGT AAATTGTGGA CTTAAAAGCC 480 CCTAAGAGAC TGGCGCAGAC TTGGAAATGT TTCCTAGTTT GACACCTCTT GCTTCTCTAA 540 GCCCAGCTTC TGGCTCTCCG ATTTGCATCT CCAAAAGGTG ATCTTTAAAA CTGATTTCCT 600 TCAGTTGCAT TTCATTGGTG TAGAAACTAA GCAGGCTGTT GCATTACAGT AATAACATCA 660 ACATTTCACC TGCCTTCGCC TTAATTATTT TTCTCTCTTG CGATGGAATC CATTTAATAA 720 GATTTACAGG TGGCAAGGAG GTGGGGTGAG CTGGTGTGCG GCTCAGATAA TCGGCCAAGC 780 TGATTTCTCC CTCATTGGGT GTCACCAGTA TAAAAACATG AACTAAAAGC TTTGCAGCGC 840 TTAAGTAATA ATAATGTCAG CATTTCACCT GCCTCCCCTT GATTATTTTT CCTCCCTCGT 900 TCTTGCCACC TGAACCTGTT TAGATAAGAT TGCCACACAG ATAGAAACCA AGGGCTCTCA 960 TTCTCTTAGA TAAGCTGCTG TTTTTCTATG GTTTGGTGTG AAAAGGGAGT GTTGCTGGCA 1020 GAAAGGCTCT GTCTCAGATC TTCCTGGTGG GGGGCGTCCG AGCCTGTGGA TCCTGGGTGG 1080 ACCAAAGGCA GCAATGGAGT AGGGGGCAGG TGGCTGTTAA GGTGGATGTG GGCACTCGGG 1140 TAGGTACCCT GGCCTGGGAG CAGAGGAGGA ACCATCTCTA AACATCTGCT CTCTCCCCTA 1200 GATGCCCCTA GGGGATCCAG GCAGGGACGA ATGGGTTTCA TTTGTTGAGG GGGAGGGGTT 1260 CTGATTATGC AGCACTAGGC AAGTCTCCAG TGTGGTATAA AAAACATTTG GGTAGCCCTA 1320 GCTTTACAAC TAGTTAGCTG GGTGGCCATG GGGAAGGAAC CCAACCCTTC TGAGCCATAG 1380 TTTCCTAAAA ACAAAGAGGT GGTTTGCTGT GGACTGAATG TTTGTGATGG CCTCCGGCTG 1440 CAGTTAATAT ATTGCAACTC TAACCTCCAT TGTGATGATG TGGGAGGTAA TTAGGGTTAG 1500 ATACTGGGAG GTAATTAAGC TCATCAGGGT GGAACCCTCC TGATGGAATT AGTGCCCTTG 1560 AAAGAGGAAG AGAGAGAATC TCCCTCTCCC TCTTTCCCTC CCTCTCCTTC TCTCTCTGTC 1620 TCTCTCTCTC 1630
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