Tag | Content |
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EnhancerAtlas ID | HS101-26834 | Organism | Homo sapiens | Tissue/cell | HT29 | Coordinate | chr20:22632890-22635110 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Tcf12 | MA0521.1 | chr20:22634049-22634060 | AACAGCTGCTG | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr20 | 22632991 | 22633067 | chr20 | 22633633 | 22633795 | chr20 | 22633796 | 22634270 |
| | Number: 1 | ID | Chromosome | Start | End |
GH20I022652 | chr20 | 22633385 | 22634189 |
| Enhancer Sequence | CTCTGCAACA CAGAAAGAAC GACCATCCTC CTCTTTTTTC TGCAGGGCCT GGACATGCCT 60 TCTTTTTTGT TCCCTTTTCG GCACCTGGCA TCATGCTGCA CACAGCAGGA GTGAAGGACT 120 ATGTTTGAGT GAATGAGTGC ATTGCCTCCT GCTTCATTTT AGCATCTCTT GTTAGGAGAA 180 AAGGGCAGAG GAAACAGCAC AAATGCCAAG CTTCGTGGAA TTCAGTGGGA GAGCCGATGC 240 ATCGGCCTTC CCTCGGTGCC TGTCACAGTG CTGGGGCTCC ACGGCCTCCC TTGCTCTGCT 300 CCTCGTGACA TCCATGGAAC AGGCACTCGA ACCCTCCCCC TCCTCTTACA TGTGGAGGGG 360 ACTCATATCC AGAGATTCTG ACTGCGATTC CCAAAGCACA CAAGCACGAG GAGGAAGGGA 420 ACCCAAGTTT GCCTGATAGA AGAGTCCAGG CTTTCTTTCT GGAGCCCATT TTCCTTTAGA 480 AGGAGGAAGT AGACCTCCAG GAGCTCTATT TCAAAGCCCT CCCCTCTGAT CTCCTTCAGA 540 TGGATGGCAC CGAGCCGGGG AGGAGCTGTT TCGGCTCCCT CCGCTCCCAA GCTGGCTTAC 600 AACTCCTGCT CTGTGAGGCT GACTCCTCCC CTTTCTCCAC ATGCCGCTGT ATATTGGAGT 660 CTTCACCGCT CAGTTCAACA TTCAGGAACC TCACTTCATT TTAATATGTT TTGCTCTGAC 720 AGAAAATTCA TTTCCCTGGA GCTGAAGCTG CTCCCCCTGC CAAGAGCTGA ACTGGCTGGT 780 GCCAGTCCCG GGGTTCTGGC TGTGCCAAGT TCAAGGATGA AGGGTAGGTC CCTTCTCCTG 840 CCATTTACCT TCCCAGATTC TTTCACAAGT TGGGTTGGAA CCAGGAACTG GAAGTCCAGG 900 AGGGTGTTTT GTTTCTCTCA TTGAGGTTTT CTAGTGAGTA CCACCCCGAA CCCCACATGC 960 GAACAGGGAC CTAAATGACT CACCCTGCAG GGGTGGAGCA GGGGCCTCCG CAGTCCCGAG 1020 TCTAACCTCC ACCAGGGCAA CCTGAGCCTG CAGCCTGATC TCCACCCCTC ATGGAAACAG 1080 CCTGGCTGCA AAGATTTTAC TGCCCGAGGG ACACGGGGAA AAGGCCACCC CTCTGCCGCA 1140 TATGAGTCAC TGGTCTATAA ACAGCTGCTG GGCGCCTGAA TGCCCCTCAC ACTTTGTTTG 1200 CCAGCCCGAA AGCCTCATAT TTCCCTGCAA CGAACTGCTA CTTTTTTAGG ATTGTAGGAG 1260 TTTTACAAGC TTTAAGAAGT TTATAGTGTC AGATTAAGTA AGATCCAGCG CTAAGAATTC 1320 GATTTCATGT TTTCAAGAGA ATTCATACAC GCGGCTCATA AATTCTGGAA CAAGATCCCT 1380 ACAGACTCCA GCATAACTGA TCTAGGAGAA ACTCTCTATG AAACCTTTCT CTTTGGTGAG 1440 TTATGGAAAA TATTTGCTGC CTACAGCCTG GGGTGATGGC AAACATTCTT GTGCAGGCCT 1500 GGTGTCGGGG TGCACAGTGA TGTGGCACAG CTGTGACCAT GCCGGTTGGT CTCGAGCTTG 1560 CGGCCTGTCA CAGGGTGTTT ACCTGAGAAT GAATCTGAGA GGCCACAGGG CTGGAACTGT 1620 GTCTCGCGGG CGGAGGAAAA TGTGCACAGC TATTTTAAAG CCGAGGGCTG TACATCTTGT 1680 TCACGGCCTG CTGTTCACAA GGACAAACAG GGCTCACCTA AGGAGAGGGA CAGTCTTTAA 1740 ACAAACCTCG TTACACTTCA AGAGTCGCTT TCAAATTGGA AAGAAAGGGG GACAAAAGGG 1800 TCTTACATGC GTCTATGATG GATGAGACAC ACAGGCACAG AAGCAGCGGC AGACTCACAT 1860 TCTCCTTGCT GCTGGGGAGC CTGAGAGACA GCCTGGTGGG GATATGCATG TGTACATGCT 1920 CATACAGATC AGCCTTGCAC ACAGATATGC ACACATGCAC ACAGACGGAC ACACAGCCAC 1980 ACATACCTTT ACACGCACAG ATGCATACAA ACCTACACAC ACGCACATGC TCACACACAA 2040 ATACACATGC ACACAGGCAC ACATCCACAC ACCTATACAC GCGTAGATAC ACAAATCCAC 2100 ACACATGCAC ATGCTCATGC ACAGATATAC ACACAGATAG ACACACATCC ACACACACCC 2160 ATACACACAT AAATACACAA ATCCACACAC ACGCACATGC TCACACACAG ATATACACAC 2220
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