Tag | Content |
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EnhancerAtlas ID | HS051-10863 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr16:84544470-84545900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:84545118-84545137 | TGTCCACCAGGTGGCGCTC | + | 8.13 | EWSR1-FLI1 | MA0149.1 | chr16:84544516-84544534 | GGAAGGAGGGTAGCAGGG | + | 6.21 |
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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 |
GH16I084510 | chr16 | 84544521 | 84545679 | GH16I084512 | chr16 | 84545724 | 84549978 |
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Enhancer Sequence | TGGCATCCTG TTATCTGGCA ATCCTCATCA AAAACAGCAG CTACATGGAA GGAGGGTAGC 60 AGGGAAGAGA AAAACCACAG TCCCTGCTGC CCCAGTAGGC TCTTGGGGGC ATGGGGGAAA 120 GCTAATGGTA AGTCAGCATC CACATTTTAC TACCTGGGAC CGAACATTTT AAATTCATGA 180 ATAGAGACTG CTTTTGATCT AAAGTGGTAC CAGGAACTAA TTCCCTAGGA ATAGTCAAAA 240 AAAAAAAAAA AAAATCACGG GAAAGGTCTG GGCTTTTCAT AGCGTAGAAA GAAGGGACAA 300 GAGGGCAGCC CTCTTCCCGC GTTCCCACTG AGCAGGTTTG AGGGGCAGCA GGAAACAAGG 360 CTGACTGCAT TGTGGCACCC CTCCAGGCTG CCTTGGACGA GTTAAGATGG GATCCGTCAG 420 CTTGGTCCCT AACCCCAGGT AAAGATGGAA CAGATGCTGG CTGTGACCAG GAGTCCTGAA 480 TTTGCCTTGC ACCATTTCCC TCCACCGGAC TGGGAGCCAC TGCGGGGCAG GAAGCTGCCT 540 TTTCCATTTC CCAAGACCGG AATCAATCAC AGCGGCTCAT CGCATCATGC ATCCTCTGCA 600 ATGGTTCCTT CCTTTCCAGG GAGGTTGGTC ACGGCCAATG CTGTCCTGTG TCCACCAGGT 660 GGCGCTCGCG ATCACCGCAA AACACATGGC TACCGTGATG GTTTTTAAAT AAGAAATCTT 720 ACAATGGTTT TAGACATAAA GGACTGTTGA GAATATGATA GAGAGTTCGT GTGCGACCCG 780 CACCCTGTTC CACTGCGCCT TAACATCTGA CATGACTCTG GTCCATCTGT CACCATGAAG 840 GAGCCAATTC ATATATGAGT AAGTCACCTG CATTTTATTC ACTCTTCCTT CGTGTTTGCC 900 TAATGTCCTT TTCTACCCCA GGTCCCACGA GACATTTAGC CATCAGGTGT CCCCAGGCTG 960 CTCCTGGCTC TCGCGGTTGC TCAGACTCTT TGTTTCTGAT GCTCTTGACA ATTTGAGGAG 1020 TCCTGGTCAG GGATTCAGTC AAGTGTCCCC CACTATTGTG ATTTAGCTGA TGGTCTCCTC 1080 GTGATTGGAC GGGGGTATGG GTCTGGGAGA CAGACCCCAG AGGTGAAGTG GCCCTTCTCG 1140 TCACATCGTT TCAAGGGCCA GAACTATCAG TGTGGCTCAC GGCCGTCGAT GTCGCCCTTG 1200 AGTACCTGGC TGAGGTGGCA CCTGTCCGCC TCTCCTGCTA TGAGGCTGCC CTTCCACTCC 1260 CCTTCTATTC TGTACTCTTG GATCATTTTT TGGCTTTTGG AAACCATTTC CTGAACGCTT 1320 GGCCATTGGA GCACTGAGTT CGGTTAGGAC AGTGGAGGTA GGGGTGAGAA TTGGGGGACA 1380 GGGTGCTGGT CACATGGTGT GAGAACAAAG TGGAAACTTA CAACCAGGGG 1430
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