Tag | Content |
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EnhancerAtlas ID | HS038-23184 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chrX:71287900-71290330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chrX:71288853-71288866 | GGCAGCTGTCACT | + | 6.04 | ZNF263 | MA0528.1 | chrX:71289465-71289486 | GGAGGAGGAGGAGAAAGAGGA | + | 10.04 | ZNF263 | MA0528.1 | chrX:71289450-71289471 | GGAGGAGGAGTAGGAGGAGGA | + | 10 | ZNF263 | MA0528.1 | chrX:71289606-71289627 | CTCTTTTCCCTTCCCTCCTTT | - | 6.25 | ZNF263 | MA0528.1 | chrX:71289248-71289269 | GGGGGAGAGAGAGGGAGGAAG | + | 6.26 | ZNF263 | MA0528.1 | chrX:71289236-71289257 | GGGGGAAAGGGAGGGGGAGAG | + | 6.34 | ZNF263 | MA0528.1 | chrX:71289233-71289254 | GGAGGGGGAAAGGGAGGGGGA | + | 6.46 | ZNF263 | MA0528.1 | chrX:71288662-71288683 | AAAGCAGGAGAGGGAGGGGAG | + | 6.57 | ZNF263 | MA0528.1 | chrX:71289459-71289480 | GTAGGAGGAGGAGGAGGAGAA | + | 6.6 | ZNF263 | MA0528.1 | chrX:71289242-71289263 | AAGGGAGGGGGAGAGAGAGGG | + | 6.71 | ZNF263 | MA0528.1 | chrX:71289477-71289498 | GAAAGAGGAGGAGGAGGAGGT | + | 6.86 | ZNF263 | MA0528.1 | chrX:71289261-71289282 | GGAGGAAGAGAGAGAGAGAGA | + | 7.02 | ZNF263 | MA0528.1 | chrX:71289480-71289501 | AGAGGAGGAGGAGGAGGTGGC | + | 7.19 | ZNF263 | MA0528.1 | chrX:71289258-71289279 | GAGGGAGGAAGAGAGAGAGAG | + | 7.1 | ZNF263 | MA0528.1 | chrX:71289456-71289477 | GGAGTAGGAGGAGGAGGAGGA | + | 7.48 | ZNF263 | MA0528.1 | chrX:71289474-71289495 | GGAGAAAGAGGAGGAGGAGGA | + | 7.92 | ZNF263 | MA0528.1 | chrX:71289441-71289462 | AGAGGAGGAGGAGGAGGAGTA | + | 8.12 | ZNF263 | MA0528.1 | chrX:71289230-71289251 | GGGGGAGGGGGAAAGGGAGGG | + | 8.23 | ZNF263 | MA0528.1 | chrX:71289447-71289468 | GGAGGAGGAGGAGTAGGAGGA | + | 9.01 | ZNF263 | MA0528.1 | chrX:71289444-71289465 | GGAGGAGGAGGAGGAGTAGGA | + | 9.09 | ZNF263 | MA0528.1 | chrX:71289453-71289474 | GGAGGAGTAGGAGGAGGAGGA | + | 9.24 | ZNF263 | MA0528.1 | chrX:71289471-71289492 | GGAGGAGAAAGAGGAGGAGGA | + | 9.51 | ZNF263 | MA0528.1 | chrX:71289468-71289489 | GGAGGAGGAGAAAGAGGAGGA | + | 9.91 | ZNF263 | MA0528.1 | chrX:71289462-71289483 | GGAGGAGGAGGAGGAGAAAGA | + | 9.95 |
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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 |
GH0XI072069 | chrX | 71289051 | 71289850 |
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Enhancer Sequence | TAGACCTTCC AGACTGAAGA AGCTTCTCTT TGATAGTCTC ACAACATTAT TGATCCTTCT 60 CTGTATTGTC ATGGCCTTTG GACATGTCAT TCACACCCTC CTAGGCAATG ACTGGCACCT 120 CTATCTCCCC AACGCTCACA CAGAGCCTGG CCAGAGCAGA TCCCTGGGAA CTGCTGAAAG 180 AATGACTGAA TGACTGGGCA GGTGAGTGGG CAGATGGATG TGGTGATCCC ACTTTAGATC 240 TCTTGCCCCA AAGTCAGAAA GCTCTGCTTT CTGGATGGCA CAGTGCCCCA AGTCTTCCAG 300 GCTGAAGCTC TAGCCAGACC CACACCCACA GTGCTTTGTG GCCATGACTA TTACAGACAG 360 GCCCCCTGTC CCAGTGAGCA GAAATCTGAT GACATCAGCA TTGAGCAGTA CCACCACTCG 420 CCTGAGTGAA GGCACTTGAG GCTGTCTAGC TCTGGCAGAG TTGGTTCCAG GAGCCACAGC 480 CCTTCCTCAC AGCCAGGCTG CTGGGGCTGG AATGGGCTGC TGAGCTAGCA CCACCTGCCC 540 GGTGTCGCTT ATCCCAGAGG GCTGCAGCAC TCACAGTGAG CGGCTGCGTA AGTGTGTCCG 600 TGTGTGTGTG CGTGTGTGTG TGTGTGAGAG AGAGAGAGAG AGAGAGAGAG CGCATGTATT 660 TGCTGTGGGA CTCATGGAAG GAGCCCTCTC ATTGGCTGCC AAGGGTCCCA GTTCCAGTCT 720 GTGAATCTCT GGGCTGCCAG CTCTGCCCTC CCCTGGGAAG GCAAAGCAGG AGAGGGAGGG 780 GAGAGTGGAG TGAGGCTTCA GGTGTGTCTG ACAAGGAAGC AGGTACACCT GGTGGCCACA 840 CTGGGCATTC TTGTGGCATC TGGCTGTGCT AGCTCCAAGT CTGCAGCCTG ACAGCTTTGT 900 GCTCTGCCCA AATTTTCCCA GATTTCTGTT GGGACTGGAG CCCAGAGCTC ATTGGCAGCT 960 GTCACTTACA GAACTGGATC CATCCCCCAG TGGAGCAGGG AGCTGTGTCA CTTAGAATTC 1020 CTGGGTAGCA CATTCCTTCA GTAGACCCTG TCACACTCCT GGATTAGGCT CTGTTATTGG 1080 CCCCGCGCTC CTGCAAGCTT CTGCAGACAG AGTGAGCGAG TGAGCGAGTG AGTGAGCCAG 1140 CGAGCGGCAG CAGGAATGAC AGCACTGAGA GCAGAGACAG CCAGGGACGG TGAGGGCGGG 1200 CGAGTCGGGT CCCGGGGGGT GCCTGTGCTG GCCCTTTCTG CAGAGGCAGA TGAAGTGGGG 1260 GCCACTTTCA GGGCTTGCTA GGGTTTCTCT TGGAACCTGG GCTGCTCGAC CCGAGTGGAG 1320 CACTGAGCAA GGGGGAGGGG GAAAGGGAGG GGGAGAGAGA GGGAGGAAGA GAGAGAGAGA 1380 GAGACTGAGA GAGACTGAGA GAAGCTCCTA GCAGGCTCTA GTCCAAGTGA GAGGCTCAGA 1440 TCTGTACAAT TCTGTGCCAG GGGCACAAGT GGGATTTGGA AGAGCCATGT GTGTGAGAAG 1500 CAAAGCTGAG GTGATGTAAG CACCTGGGGA GGAGCACAGG CAGAGGAGGA GGAGGAGGAG 1560 TAGGAGGAGG AGGAGGAGAA AGAGGAGGAG GAGGAGGTGG CAGCGGCCGC CGCGGTGGCT 1620 GCCAGTCCAG AGCAGAATGA TGGGCAACTC TCACCACAAG CAACCGAGGA GTAAAAGCCA 1680 AAGCAGGATG CATTCAGCAA CAGGTACTCT TTTCCCTTCC CTCCTTTTCC GGGGCTCCTA 1740 CAGCCAGGGC CTCCCAGCTG CTGCCATGCG GGGCCCCTGA CCCTTGGCGT GACTTGCAGG 1800 GGCTGGCAGG GGGCAGGGAG AGAACCCGAG GGAAATGAGG GTGAACTTCC AGCTCCCCTG 1860 CTCCTGTGAC AGGCTGAATT GCATAAGTCA GAGCATCCTG AGCTGGGAGG GGCCAGCCCC 1920 TTCGCCGGCA ACCCTGTGTA GCCTCTGGAG GGTGGCTGGA GTGTCAGAGA AGTGAGCAGC 1980 GTGCCAGTGA CTGAAGTTCA TGGCTAGGAC TGTGCTTTCT CCCTGGATCC AGTAGGCAGA 2040 ATCTTGGAAC CATGCATGGC TTATCCTTTA CTAGCCGAGC CTCCTTTGTT ATTCAAACCT 2100 TCGTCTCCCC CCACCCCAGC CCCCATACCC GCCCTGAACA TGTACACCTA CACCTCTCCT 2160 GGCTCTACCT CATATGCTGC ATGCATGGAA TGATCCAGAC AAATCTGTTT CTTGCTGTGT 2220 AATGCCCTGC CCCCCACCAC CCTGCCCCAG CCCTGACAGA GCTCTCCTCA TGCATGGGCG 2280 AGAAGAGCAT TTGCCGGCCT TGAGTTTGTT GTTCCCCTAC CTCTGGGTGT GCTCTGCTTT 2340 GCCCCTTCCT TGCCCCTCTC CAGATATGGA CTCAAGGGTG CTGGCATAGT TCTCCCCAAC 2400 AACTCCTTCC TGGATGCTGA CACTGTGGAA 2430
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