Tag | Content |
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EnhancerAtlas ID | HS003-30972 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr22:29260560-29261710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr22:29261141-29261156 | GGTAAATCATTAACT | - | 6.71 | HNF1A | MA0046.2 | chr22:29261141-29261156 | GGTAAATCATTAACT | + | 6.82 | HNF1B | MA0153.2 | chr22:29261142-29261155 | GTAAATCATTAAC | - | 6.46 | HNF1B | MA0153.2 | chr22:29261142-29261155 | GTAAATCATTAAC | + | 6.82 | SPIC | MA0687.1 | chr22:29261598-29261612 | AGAAAGGGGAAGAA | + | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 29261088 | 29261244 | chr22 | 29261004 | 29261197 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I028865 | chr22 | 29261004 | 29261197 |
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Enhancer Sequence | AGCCACCAAG TTTGTGGTAA TTTGCTACAG CAGCCCTGGG AAAATACTAA TAGGCAGGAA 60 GCTGGAGCGG GGAGCAGCAA AGTCAGGGGA CAGGGAGCCC AGACTAGAGG CTGGAGAAGA 120 CCAGGCATGT AGCAGGATGA GGCGTGCTCA CCTCCCACAC GCACCAGGAG CAGGGCAGTC 180 CTCTTACTCA TAGGCAGGTC CATTCCCCCA GGGCTAGGAG GATGGGGTCT CTACCTTCAC 240 TATTTTCTTT AGAAAGAAGA AAGAAAGAAG AAAGATAGTG ATGGCGGTAA GGACAACAGG 300 GCCCTCGGGG GCACATGGCT ATGCTGTGGC CTGGAGAGAG GCAGACTCTT CTCAGAGGAG 360 GCTAAGGGCC TCTGGCTAGA GCATGGCTAC AAGCAAGGTG GCTAACATGA AGAGACCATG 420 GTGCAGAGGC AGATGCCAGC AGGCTAAAGG ACAATTCTGG AATGGGGCAG TGGGAGGGGT 480 CCTGTGTCTT TGGGCTTCTT TGATCCCTGA GACACTTTGG ACGGGACAGA GCCTTGGCCA 540 CCAACGGGGT CATGTCTGTT TAAACAAAAT TTAACACAGG AGGTAAATCA TTAACTCACT 600 GAAGAAACAA ACAGGAGTGC AGGCCATATC TCTAGCACCA GGATTCAAGA GCCACGGGGA 660 TGTTAAGAAC TCCTGAATAT CAGAAGTGGC TGCCACTCAT GGCTTCTGTA AGTGAGTGAA 720 AGCATTTGGT GAGCACCTTC TATAAGCAAG TCTTCGTGCC AGGTGCTGTG GGAACAGATG 780 CATGAAGAGG CTCAGAGTCT GACCTGAGCT TGGAGCTGGG GGAATACGAG CTCACAGCCA 840 TTGTGAGCAT GCCCATGCCT GTCTCCAGGC CCACCACGGC CCATCCATCA TCTCATGTAA 900 TTCTCATGCC TCTGAGGTAG GGCAAGGATT GCCTGCATTT CATAGACAAG GAAACCCAAG 960 CTCAGAGAGG GAGAGCAACT TGCCTCGGCC ACACAGCTTG TCAGTGGTGG AGAAAAATAA 1020 ACAGGAGCTG GCTTTTGCAG AAAGGGGAAG AAATTGTTAG GGTTCAAGGA TGTGTTTAGG 1080 AACTTAAGGG CAGGAAGCAC AACTTCCTGA AAGACAGGAG CCAGGTCCAG CAAAGCCATC 1140 AGGAGGCAAG 1150
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