Tag | Content |
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EnhancerAtlas ID | HS088-05258 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:212016000-212017350 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CUX1 | MA0754.1 | chr1:212016809-212016819 | TTATCGATTA | - | 6.02 | CUX2 | MA0755.1 | chr1:212016809-212016819 | TTATCGATTA | - | 6.02 | IRF1 | MA0050.2 | chr1:212016667-212016688 | TCTTCCTTTCACTTTCACTTA | + | 7.86 | PRDM1 | MA0508.2 | chr1:212016675-212016685 | TCACTTTCAC | + | 6.02 | RAX | MA0718.1 | chr1:212016701-212016711 | GTTAATTGGC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 212016062 | 212016200 | chr1 | 212016200 | 212016763 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I211843 | chr1 | 212016343 | 212016742 |
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Enhancer Sequence | AATGGTAAAT GAGCATTGGC TTCTGCCCAG TCATCAGTTA CATTAGTCCC TAACAAGAGC 60 CTTAGTCATC CTTTGAAGCT TTGAAGTCAG GCATTGACTT CTCTCTAGCT GTGAAAGTTC 120 TAGATGGCAT CTCCTCCCAA TATAAATCTA TTCTGTCGAC ATTGAAAATC TAGGGTGTAG 180 TGTAGCCCCC TTCATCAATC ATCTTAGCTA GATCTTCTGG ATAACTTGCT ACAGTTTCTA 240 CATCAGCACT TGCTGCTTCA CTTTGCACTT TATGTTATGG AAATGGCTTC TTTCCTTAAA 300 CCTCATGAAC CAACCTCTGC TAGCTTTCAA CTTTTCTTTT GCAGCTTCCT CACCTGTCTC 360 AGCCTTCATC AAATTAAAGA GTTAGGGCCT TGCTCTGGAT TAGACTTTAG CTTAAGTAAA 420 TGTTGTGGCT GATTTGATCT ATCTAGACCA CAAACTTTCT CCCTATCTGC AGTAAGCCTG 480 TTTTGCTTTC TTATTCATGT GTTTACTACA GTAGCACTTT TAATTTCCTT CAATAACTTT 540 TTCTTTGCAG TCACAACCTG GGTAACTGGT GAAAAAGGCC TAGTTTTTGG CCTGTCTTGG 600 CTTTCAACCT GCCTTCCTCA CTAAGCTTCA TTATGTCCAG CTTTTGATTT AAAGTGAAAA 660 ATGCAACTCT TCCTTTCACT TTCACTTAGA GGCCATTGTA GGTTAATTGG CCTAATTTCA 720 ATTTTGTTGT GCCTCAAGGA ATAGGGAGGC TCAAGGAGAG GAAGAAAGAT GGGAATGGCC 780 AGTTGGTGGA AAGAACAGAA CACACACATT TATCGATTAA GTTCACCCAC CTTCTATGAG 840 CAAGGTTCTT GGAACTCCAA AACAATTACA ATAGTAACAT CGAAGATCAC TGATCACAGA 900 TCACCATTAC AGATATAATA ATAATGAAAA GGTTGAAAAT ATTGTGAGGA TTCCCAAAAT 960 GTGACACAGA GACAAGAAGT GAGCACATGC TGTTGGAAAA AATGGCACTG TTAGACTTGC 1020 TTAACACAGC GTTGCCACAA ACCTTCAATT TGTAAAGACT TGCTCAACAC AGCGTGGCCA 1080 CAAATCTTCA ATTTGTAAAA AGCACAATAT CTGCAAAGCA CAATAAAGTG AAGTGCAATA 1140 AAACGAGGTA TGCTCAAATA AACTATCTGG TCTGAGCCTT GGTTTCCGAA ATCAAAGGCT 1200 ATAAAGAAAA GTTATGTCTC TTTAACTTGC TGCCTTTAGG CATTTCAACC ACCTCAGATC 1260 ACTGTGTTCC CCAAGGAAAT TGATCTTCTT TGTAGCCTAA CAACCATACC TAACCCCACA 1320 CAGATTCGCT ATAAATGAAG CCAAGAAAAT 1350
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