Tag | Content |
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EnhancerAtlas ID | HS101-16583 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:19016420-19018970 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2B | MA0660.1 | chr16:19017024-19017036 | GCTAATAATAGC | + | 6.07 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 19016606 | 19017680 | chr16 | 19017780 | 19017800 | chr16 | 19017800 | 19017874 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I019005 | chr16 | 19016524 | 19018195 |
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Enhancer Sequence | TATTTTCTGA GACGGAGTCT CGCTCTGTCG CCCAGGCTGG AGTGCAATGG CAAAATCTTG 60 GCTCACCACA AGCTCTGCCT CCTGGGTTCA CGCCATTCTT CTGCTTCAGC CTCCCAAGTT 120 AGCTGGGACT ACAGGCACCC GCCACCATGC CCGGCTATTT TTTTGTATTT TTAGTAGAGA 180 TGGGGTTTCA CCATGTTAGC AGGATGGTCT TGATCTCCTG ACCTCGTGAT CCACTCGCCT 240 CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA CGCCTGGCCC GCATGTTAAA 300 TACTTTAAAT GGCCTGGTAC AAGGTAGGCA AGTACTCAAT AAATCTTAGC CAGTGTTGTT 360 CATGTTGTTT GCAACTCCTT CCTCACCATC ATGCTGATGA GGCCCATGGT ATTAGATCCT 420 CCATTCCCGA GATGAGAAAA ATGTGACTCT GAGGCAGCTG TGGTCTCTCC TGGGGTGGCT 480 TGGCTGGTGG GTGACAGGCC AGTATTTTAA ACCAACCCAG GCTCCAGCCT GGGGCCCCTG 540 ACCCCACAGC TGTTGAATAT TCAGTAGGTC CATGCTGTTC TATATTCAAA GACCTTTGTT 600 TGTGGCTAAT AATAGCTCTT TGTTTCTGCT TGCAGGAGGG TAGCCTCCAT GCAGGGCTTA 660 GACCCTTTTC CTTTTCAGGG ACCACACCCA CCCTACCCTC ATATTGGCTC TAGGGAGCCA 720 CTGCCACTAA TGGAAGTGTG TCATATCCTC AGGGTGTGCC AGGCAGGGAG GTAGAAGGGT 780 GGGTGAGGCT CGTAGACTTG CACATGGTGA TTGGCAGGGC CCCAGCCACG TGTCCATGTG 840 TCATCTACAG TGGGACAGCT GCTCCATTGT GTCTGAACTT GCCTATCCGA GAAAGGCAAA 900 GATTACAGTG TCAGAGCCAG GCCTTGACCG GTCCCCACCT GGCCCTGCCC CTGCCCATCC 960 TCATCCGGTT GGTGCCTTTA TGGAGCTCTG TGTGTGCCGA GCACTGCCTG GGACCTTCTA 1020 CCCATGTGAT CCCCTTTAAT GTTCATAAAC AGGCTGTGTA GCAAGTCCTG ACCCCAGCCT 1080 TGCCCTTGCA GCCTCCAGGG TGACCTTTTT TTTTTTTTTT GGACGGAGTT TCGCTCTTGT 1140 TGCCCAGGCT GGAGTGCAAT GGCACGATCT CGGCTCACTG CAACCTCCGC CTCCTGGGTT 1200 CAAGCGATCC TAAATAGCTG GGATTACAGG CACGCGCTAG CGTGCCCAGC TAATTTTGTA 1260 TTTTTAGTAG AGACAGCGTT TCTCCATGTT GGTCAGGCTG GTCTTGGACT CCCAACCTCA 1320 GGTGATCCCC TTGCCTTGGC CTCCCAAAGT GCTGGAATTA CAGGCGTGAG CCACCGTGCC 1380 CGGCCCAGGG TGACCTTTTA AAATGCAGTC AAAGCACAAC ATCCCAAGGT CCTGCCACAG 1440 TCTACAAAGC CTGACTTGGT TCGACCCCAG CCACCCCTCT GACTTTAACG TTTCCATTCT 1500 CCCTGTCCTA AATACCTATT GTTGCTCAAC ACACTGCTCC AAATGTGCTG GCTTAAGCCA 1560 TGTTGTTATT TCTGCTGATT CTGTGCATCA GGGACGATGC AGGGCACGGG GGAGCCCGCT 1620 TGCACTGCTG CCTGGGATGT CTGCTGGCGC TGGAGCACCC AAGATGGCCT CATCATGGCG 1680 ATGCCTGGTG AGGATGCCCC AGGGGTTTTT TTTGTTTTCT TTTGTTTTGC TTTTTTGAGA 1740 CAAAGTCTTG CTCTGTCGCT TAGGCTGGAG TGTAGTGGTC CAATTTCGGC TCACTGCAAC 1800 CTCTGCCTCC CAGGTTCAAG CTATTCTTCT ACCTCAGCCT CCTGAGTAGC TGGGATTATA 1860 GGCGCGTGCC ACCACGTGCA GCTAGTTTTT TTTTTTTTGT ATTTTTAGTA GAGATGGGAT 1920 TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCCCACCTC AGGTGATCCG CCTGCCTCGG 1980 CCTCCCAAAA TGCTGGGATT ACAGGTGTGA GCCACCGTGC CTGGCTGTCC CAGGGGTTTG 2040 AAGACACGAG CCTGGGGCCT TGGTTCTTGC AGTCACCCAG GTTGTTGGTT CTTTTTGTAG 2100 GCTTAGGGGC TCTTCCTCTC CACCTCATTG TCCTAGGCAG TTGGACTTCC TACCAGGTAA 2160 CCCTGGCCCG AGAACACAGA AGTGGCTACT GCAAGGCCCT CTTATGACTT TGGGCTGGAA 2220 ATGGCAGAGC ATTACTTCCA TTGAGTCCTT TGGTTAAAGC AAGCACAGGT CCTGTGCAGA 2280 TTCAAGGAGG GGACCACGCA GAGGGCCAGG CCAGTGTGGC TCATTGGAGG CCACCAACGA 2340 AACCGCCCAC CAGGTTCTTG CTCATTAACT CTTCCTCCAA CCTGTCACAC ACTCTTCTGC 2400 CGCTGGGCCT TTCCACTTAT GGGTTCCCTC TGCCTGGGGT GCTTTTCCCC AAATATCCAG 2460 GGGTCTCACC CCTTCCCTTC ATTCAGCCTT AGCTAAATGT CACCTTTAAA GAGAGACCGA 2520 GATCACGTGC CACTGCACTC CAGCCTGGGT 2550
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