Tag | Content |
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EnhancerAtlas ID | HS101-28669 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:24901400-24903830 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxo1 | MA0480.1 | chr22:24903104-24903115 | TGTAAACAGGA | - | 6.62 | POU2F2 | MA0507.1 | chr22:24903662-24903675 | ATATGCAAATGTC | - | 6.19 |
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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 |
GH22I024503 | chr22 | 24899088 | 24904361 |
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Enhancer Sequence | TCTGGGTCAT TCTTTTCAGG CTGGTCAGAG TCCCCAGAGA TTTTTCTGCC CTTGTGCCAA 60 GAAGGGAAGG AGAACAAAGG TTCAGCATGC TGATGTTTAC TCAATCCCTC TGTTTTGACA 120 CTTCACTTGC TTTCATCTGC CCTGCTCCAA AGCCAGAGAG CCTCTGCTGA ACCATCTCTG 180 GAGGATGAGC CTCTGGCCTT CTTCTGGGGT AGATGGGGCA GGTCCCAGCC TCTTGGTGTG 240 GAGAAAGGAC CTGGATTTCT AACTGCTTCT TTTTTTATTT TTATTTTTAT TTTTTTTTGA 300 GGTGGAGTCT TGGTCTGTCA CCCAGGCTGG AGGGCAGTGG CGCGATCTCA GCTCACTGCA 360 ACCTCTGCCT CCTGGATTCA AGCGATTTTT CTGCCTCAGC CTCCTGAGTA GCTGGGACTA 420 CAGGCCCGTG CCACCATGCC TGCCTGATTT CTGTATTTTT AGTAGAGATG GGGTTTTGCC 480 ATGTTGGCCA GGCTGGTCTC GAACTCCTGA CCTCAGGTGA TCCACCCACC TCAGCCTCCC 540 AAAGTTCTGG GATTACAGGC GTGAGCCACC GTGCCTGGCC CTAACTGCAT TTTTTTTTTT 600 TTTTTTCAGA CGGAATCTTG TTCTGTCACC CAGGCTGGCA TGCAGTGGCG CATTCTCAGC 660 TCACTGCAAC CTCTGCCTCC TGGGTTCAAA AAATTCTCCT GCCTCAGCCT CCTGAGTAGC 720 TGGAATTACA GGCCTGTACC ACCACACCCA GCTAATTTTT GTATTTTTAG TAGAGACCAG 780 GCTTCACCAT GTTGGCCAGG CTGGTCTCGA ATTCCTGACC TCAGGTGATC CGCCCACCTC 840 GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACTGC GCCCGGCCCC TAACTGCTTC 900 TTAAATAGAC CTTTGACCAG TCCTTGTTTA TCATACTTCC CTGCTTCCCC ACCTTCAGAG 960 GTACCTGGTG CCCCTGGGTC CTGAGCTTTG GATAAGCAGG AGATCTTCTC TACTGCTAGC 1020 GGGACTCAGT TTTCTCTGAT CTGCTGAGAG ATTTGCCTGC ATCTTTCCGC CTTCCAGCTT 1080 CCCGTGTTTC CGTGCCTCAG TGCACCATCC TTGTTGGGTA TATGCCTTTG CATGAACATT 1140 GCTTTCCTGT CATGTTAATG GGGTTTCAGG AAAGAACACG TGTCTGTGTC CCAGAAGTTC 1200 ATGTCGTTTT CCTATTTTTG TTACCTTTGT ACTCTCACTC TTCATTAGAC TATGAGCTCC 1260 ATGAGGATAG TATCTGTGTT TGTTTTTCCC AACTCTCCAC CCACCCCTGT TTCATCTTTA 1320 GTGGCAAGAA TAATCCCTAG TGCATGACAG GCACTACAAA TTAGTATTGG CTGGATAGTT 1380 GAACTAACAT CTCCCCTTTC TTGGATCTGG AACTCCCCCT CATTTATCAA AGTCTAGCAC 1440 AGGTACCCCT CCTTTGTGGG GCCCTGGGGA CTCCCCCAGG ACTCCCCCTG ACCACTCTGT 1500 ATTGCCAGGT TGTGTGGCCG CACCAGGTTC TAATTCATCT CCTTCCCTCT AGGCTGGCAG 1560 TTCCTGAGGG CCAGGTGTTA GGTCAGTGCA TGTGGAACCT CGTCCCCTCT AGTTGAAGAA 1620 CTGTAGTTGG GACTTTGCAG CCAGCCTCAC CCAACCTCAC TTCCACATCC TTCTTTTGAA 1680 AGTGTGTTTA CATTAGAGTG GTTGTGTAAA CAGGAAAAGA AGCTGCTTAT TCTCTGGGGG 1740 CACTTGACTC ACTCCTAATG CTCTGAAAGC TGAGAATTAA TGGTCATTAA GGAGCATTTG 1800 TGTTTTCAAC AGCTTTTCTG TTGGCTTCCT TAAAATAATT CATCTCTCTT CACAGAAGGC 1860 GAGCCTGGGG AGCCTTGAGC CTGCTACCAA GGCCCCCAGG ACTGTTGCTG GCAGTGCCTG 1920 CCGCCTGCTT GGCAAGATGG TGGTGGTGCC ATTGGCGGGA TATTTACTGT GGTACTCTCT 1980 TAGGACCAGG CTTCCTGGGA CCGGAAGGAA TTGAGAGGCT GAGGCTTCTC TTCCTTCTCT 2040 GTGAAATAAA GGGGGTGACA CCAGCTTAGG GATGTTGGAG ACGATCTGCC TATTACGAAG 2100 ATAGGAGTTA TAAAGAAATA CTTTTTAGGC AACTAGAAAG GAGTAAAAGG AATAAAGGAG 2160 TAAAGGTTCT CAGTGGAAAT TTTCCTGTAA TAAGAAGCAA CTCCTGAACC ATTTCTTTTC 2220 TAACCGAAAA GGCGGCTTAA AGAGCCAGGC CAGCAAGCTT TGATATGCAA ATGTCGGCAA 2280 TTAGAAACTA GGTCCACCCA ACATGGCAAT TCCTGCCCTC TTCTCCTTGT CACCACCTGT 2340 GCCAAGTGTC ATGACCGCCT CCAGATAACT CATACATGTT CAGGACATCA TGGCAGCTCA 2400 CGTTTGCATA TTAAAGGGCT AAGGTGGGAG 2430
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