Tag | Content |
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EnhancerAtlas ID | HS101-18834 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:46163060-46164090 |
Target genes | Number: 22 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf12 | MA0742.1 | chr17:46164070-46164085 | TAGCTGGGCGTGGTC | - | 6.33 | Nr2f6(var.2) | MA0728.1 | chr17:46163212-46163227 | AAGGTCAGGAGTTCA | + | 6.04 |
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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 | ACATAGTGTA GAATTTTTTA AGTTAAACAT CTAGCAAGCA GACTAGAGAG AGAACTACTG 60 AGAAAATGTC AATTTTAAGA AACCAGGCCA GGCGCGGTGG CTCACGCCTA TAATCCCAGC 120 ACTCTGGGAG GCTGAGGAGG GCAGAATCAC CTAAGGTCAG GAGTTCAAGA AAAACCTGGC 180 CAACGTGGCG AAACCTCGTC TCTACTAAAA ATACAAAAAA AATAGGCTGG TCACGGTGGC 240 ATGCACCTGT AGTCCCAGTT ACTCGAGAGA TTAAGGCATG AGAATTGCTT GAACTCAGGC 300 GGCAGACATT GGCAGTGAGC CAAAATCACG CCACTGCACT CCAGCCTGGG TGACACAGCG 360 AGACTCTGTC TCAATAAAAA ACAAAACAAA ACAAAAAAAA CCCAAAACTT GTTTACAGTG 420 TCCCAAGGAA TCCAGGAACA GTGTAAATCT GAATCAAGAG TAATTAATTC ATAGCTCAAT 480 TTTAAGAGAA AGAGTACTGT TGTGATTTTC CTCACCCACC CTCCACCCCT GCACTGAGGA 540 GCTAGAAAAT GTAAAGAAGC AACAATGCTA CTTGACTGCA GAAGGCAGTA ACATAACAGA 600 CACAAGCTTA GGCATTTCAT TTTGGTTTGA AATAGTTTGT ACTGTGAAAG GGTACGAGAA 660 GGCTTCAAGA AGCCAGTATG GCCACAGCTC TTGGCTGCCA CCATAAACAT GAACTATGAA 720 GTGCTATGCT AGGAACTTCC ACGATTCTGA TTTCTTGCCA GTTTGAAAAA CCAAATTATA 780 AATGTGAGGC CATGGTAACA CCTACAGACC TAAGAAACTA AACCAGTAGG GTTTCTAGCT 840 AAATGCCAAG GTGAGGCATT TAAAATGTTG GTCAGGGCTG GGCATGATGG CTCACACCTG 900 TAATCCCAGC ACTTTGGGAG GCTGAGGCAG GCAAATTACC TGAGATCAGG AGTTTGAGAC 960 CAGCCTGGCC AACATGGTGA AACCCTGTCT CTACTAAAAA ATACAAAAAT TAGCTGGGCG 1020 TGGTCGTGCA 1030
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