Tag | Content |
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EnhancerAtlas ID | HS101-46033 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr9:115033410-115035180 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr9:115034028-115034049 | AAAGAAAAAGAAAAAGAAAAT | - | 6.01 |
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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 |
GH09I112271 | chr9 | 115033684 | 115034792 |
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Enhancer Sequence | GTTCCTTTTT AAGTACTGAG GCATTCATTA AAACATAGAC ATGCACATAT ATGTCATATT 60 TAATTCTGAG GCACAGTCTG AGTATCCCTT ATCCAAAATG CTTAGGAACA GAAGTGTTTT 120 AGATTTCAGA TTTTGAAATA TTTAATATTT GCCTTAGATA CTTACTAGCT GAGCATCCCT 180 AATTCAAAAA TCTGGAATCC AAAATGCTCC AGTGAGCATT TCCTTTGACT GTTATGGTGC 240 TCAAAAAGTT TCAGATTTAG AGCACCTCAT TTTCAGATTA GGGATATTCA ACCTTTATCA 300 TAAAATAAAG ACAGGCGTAG TGGCTCACGC CTATGATCCC AATACTTTGG GAGGCTGCAA 360 CGGGCAGATC ACTTGAGGTT AGGAGTTTGA GACCAGCCTA GCCAATGTGG TGTAACCCCT 420 TCTCTACTAA AATCACACAC AAAAAATTAG CCAGGTGTGG TGGCAGGTGC CTGTAATCCT 480 AGGTTCTCAA GAGGCTGAGG CAGCAGTATC ACTTGAACCT GGGAGGCAGA AGTTGCAGTG 540 AGGTCAAGAT CACACCAGTG AACTCCAGTG TACTCCAGCC TGGGCAACAG AGCAAGACTC 600 CGCTTCAAGA AAGAAAAAAA AGAAAAAGAA AAAGAAAATA GTTTATAATC TTCAAATACA 660 GAATATTTTT TAAAAATAAG GGACAAAGGA TCAATTATTC AAATTATGGA AATCTGAGAA 720 CTTCCTACCC TGAGTCAATA TTGATTTAAG TCATTCAAGT GATTTGATAT CTGTAGTCAC 780 TGTACTAATA GTAGATACCT GAAGAATGAC TCAGGAAAAA CTGAGCTGGC AAAAGCCCCT 840 TGACATTTAT ATTTTATAGT ATACATAGTT TCCTCTTAAC AGGAATAAGA TACTTACAAA 900 GCTTTAAGGT GGTAGATTTT GTCCCCCATC TCACTCTTTT TATTTTTTAT TTTTTTTTTG 960 AGACAGAGTC TCACTACACT GGACCGCAGT GGCGTGATCT CAGCTCACTG CAACGTCCAC 1020 TTCCTGGGCT CAAGCAATCC TCCCATCTCA GCCTCCCAAG TGGCTGGGAC TACAGGTGGG 1080 TGCCGCCACA CTTGGCTAAT TTTTTACAAT TTTTGTAGCA ATGAGGTCTC ACTATACTGC 1140 CCAGGCTGGG TCTTGAACTC CTGAGCTCAA GTAATCCTCC TGCCTCAGCC TCCCAAAGTG 1200 GTGGGATTAC AGGCATGAAC CACTGTGCCC AGCCTTTGTC GCCCTATTTT AATGATTAGT 1260 TATAAACTAT AGACATTAAC CGTTCTGAGT CCTCAAAATA CTGGTAAGAA CATCTCAAAT 1320 TTAAAACGCA GGAACCACTC CTGATCCAAA TCAACACAAA TTTCTAGTTA GACAATTCAA 1380 TTCTTTTTTT ACTACAGAAG AACATATTTA TTTATTCATC CATCCATCCA TCTATCCATC 1440 CATCCATTTT TTTAACAGAT AGGGGTCTTG ATATGTTGCC TGGGCTGAAA TGCAGTGCCT 1500 ATTCACAGGC ACGATCCCAC TACTGATCAG CACAGGAGTT CTGACCTGCT CTGGTTCTGG 1560 TCTGGGCCGG TTCACCCCTC CTTATGCAGC CTGGACCATA CTGATGCCAA ACTTAGTGTG 1620 GATACCAGAT CGGCTTAGTA CACTACAGCC CAGAATGCCC AGACTCAAGC AATCCTTGAG 1680 GCAAGTGCCA CCAAGACCAG GCACAAGAGC ATTTAATTAG CAAGCATATA TCAACCATTT 1740 CAACTTATGT ATAAAACATT TACAATTTAT 1770
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