Tag | Content |
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EnhancerAtlas ID | HS003-33529 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr3:142705720-142707080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:142706106-142706125 | ATGTGCCCTCTAGTGGTTA | - | 6.28 | Foxq1 | MA0040.1 | chr3:142706351-142706362 | AATAAACAATA | - | 6.62 | IRF1 | MA0050.2 | chr3:142706014-142706035 | AAAGAAAAAATAAAAGCACAT | - | 6 | Six3 | MA0631.1 | chr3:142706944-142706961 | GGAAGTGATATCCTATC | - | 6.08 |
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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: 2 | ID | Chromosome | Start | End |
GH03I142988 | chr3 | 142705843 | 142706042 | GH03I142987 | chr3 | 142706642 | 142706843 |
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Enhancer Sequence | TGGCTTACCC CTGTATTCCA GCACTTTGGG AGGCCTAGGT GGGTGGATCA CCTGAGGTCT 60 GGAGTTCGAG ACCAGCCTGG CCAATATGGT GAAACCCCAT CTCTACTAAA AACACAAAAA 120 AGTAGCCGGG CATGGTGGTG GGCGCCTATA ATCCCAGCTA CTTGGGAGGC TGAGGCAGGC 180 AGGAGAATCA CTTGAACCCA GGGCAGGGGG AGCCGGGGGG AGGCGGAGGT TGCAGTGAGC 240 CAACATCACG CCATTGCACT CCAGCCTGAG CAATAAGAGC AAAACTCTGT CTCAAAAGAA 300 AAAATAAAAG CACATTTCTC TTATTCTTTG ACATTCTCTT GTAATATACA TTTCAGTTAC 360 ATGAAATTGA AAGACAACCA AATGCAATGT GCCCTCTAGT GGTTAAAGAA AATAATTTAC 420 AATCCACCTC TCCTGAGCCA AATACACAGA TCAAATGTAA TTTTTCAAAG CCTACATTCA 480 GTTATGTGGA TAACTTAATT GGTTATTTCA GTGTGGCTTT TGTCCTCTTA TGAAAACATG 540 GCATATCAAA AAAATTGTCC ATCTTATAAA ATAATCATTT TTCTCTATTT GCAAAAACAA 600 AAAAAGTATT GACCTATTTA CCTGTTTGTT GAATAAACAA TATATTAAAA TAGACCAAAG 660 AATGGGGAGT GAAAAGTAAA TTTCCTCCCA CCCCTGACCC TCAGAAGCTA AAGATGGCTT 720 TCCTAGTGGC AAGCACAGTT GCCAGTTTTT AAATAAATAT ATTGTGTATA TGCATAAACA 780 AATACACGTT ATATTAGTTA TCTACTGCTA CGTAGCAGAT TACCCAGAAC TTAGTGGCTC 840 AAAACAACAA ACATTTATTA TCTCACATTT TCTGTGGGTG AGGAATGCAG CAGCTTAGCT 900 AGGCCCCCAG CGCTGGGGCT TTCCCAAGGA TGTAGTCAAG CTGTCAGCTG GTGCTGCAGT 960 CAGCTCATGT CTCAGCTCGG GAGGATCTGC TGTCAGGCTC TCTCAAGGGG TTCTTGGCAG 1020 GATTTAGTTC CTCACACGTT GTTGGGCCGA GGGCCTCATT TCTTCACTGG CTTTTGGCCT 1080 GAGGCTTCCC TCAGTTTCTT GTTACACGGT CCTCTCCATA GGACACCTCA CAGCATGACA 1140 GTTGGCTTCA TCGAGTAAAT AAGAGAGAAG AGCCAGAAAA GGCAAGCAAG ACTAGAAGCC 1200 AAAGTTTCTT GGTAACCTAA TTTCGGAAGT GATATCCTAT CACATTTGCT GTGTTCTGTT 1260 TGTTAGAAGC AAATTCCTGG GTTGAACCAT ATTTAAGGGG AGAGGATTAA ATAAGGGCAT 1320 GGGCACCAGG AGTAGGAGAT CACCGGGGGC CATCTTAGAA 1360
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