Tag | Content |
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EnhancerAtlas ID | HS139-17763 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr14:105346760-105349060 |
Target genes | Number: 15 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_24889 | chr14:105347880-105350475 | Colon_Crypt_3 |
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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 |
GH14I104882 | chr14 | 105348701 | 105348970 |
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Enhancer Sequence | AGGTAGGCCC AGGCAGTGCG GATGGGGTGA GCACACAGGG CCACTGCCAG GCCCTCTGCC 60 CCGCACCTGC CTCTCTGCAC CCCTTAACCC TCTGCATGCA TATACCATGT ACACCCATAC 120 CCCTCACCCT TTGCACACAC CTACCCTTGC ACATGCACAC CCCTCACCCA TTGTGCACAC 180 CTACCCTTGC ACACCCACAT TCCTCACCCA TTGCACACAC CTACCCGTGC ATGCCTGCAC 240 CCCTCACTTC TGTACACACC TACCCATGCA TGCCTGCATC TTCGTTATAC ACACCCTACT 300 CATGCACACC CACACCACTC ACCCCTGTGC ACACCTACCC ATACATGCCC ATAGCTCTCA 360 CTGCTGTGCA CAGACCTATC ATGCACACCC ATACTGCTCA CCCCTGTGCA CTCACACCCC 420 CACCCCTGTA CACACATCTA CCTGTGCACA CCCACATCCC TCACCTCTTA CCCCACACAC 480 ACAGCTACCC ATGCACACCC ACACTGCTCA CCCCTGTGCA CACCTACCTG TGCACGCCTG 540 CACCCCTTGA GCCCACAGTT CTTGTGGGGT TGGTGGGCCA CCAGCTGGGC ACCCTCTGTC 600 CCCAGTGGTG AGAGGCAGGT GATGGGGGGG TGAGGCTATG CTCCCTAGTA TCAGGCATTT 660 GGACTGGATT CTGCAGACCG AGCCAGCAGG GCTCAGGGGT TGGTGGTTTC TGATGAAACC 720 TGATTTGCGC CTTTGGCAGT CAGTGCAGCG GGTAGGCAGA AGTCTGGGAG GAGGACAGCT 780 GCACGAGGGT CCGCGTGGGT CCGGTGGGCA CAAAGGGAAG GGAAGGAGCG AGAGTGAGAA 840 AGTGCCTGGT GGGGTGTGGA GGGGTCGGGG TGGGGTATCC AAGCCTGAGG CCCCAGACTT 900 GAGTTCTGGT TAGACAGGGG TGTATCCGGG GATCAGGCTC TCGGCTCCCA CCTCGGTCCA 960 GGAGGGGTCA CCCTGCCACC CCCAGCTTTG GCCCCATGTC TGCTGTGTTC TGCTGTCAGC 1020 CCACACATCT GTGTTGTACA GCCGCAGCTG CCGGTGTCTG GTTGGGATGC AGGTCCGCCC 1080 AGAATGGAAG ACCGCTGGGG ACTGGGAAGC TTTCCAGAAA GCCATCTGAG CTCCCCAGAG 1140 CACCTGTCAG TGTCCAGACT GTGAAACACA TGCAGCTGGT GACAGCCAGT GTGGGGCTGT 1200 CCCGGAGGTC ATGACAGGTG CAGCCAGCTG GGCAGCCTGG CTCCTTGGCT CCGTTAGAGC 1260 GAGGGCAGCA CATTGTGGGG ACCAAGGAGG AGTTCAGGGC CGGCAGCAGA TGGGGACTGC 1320 CTGGTAGCAG ATGCCCCTGC CTCAGCAGCC CCTGGGTGTG TCCCTGGGTC AAGAGGGAGT 1380 CCCCAGGGAG GGGTAAGGCG TGTGTGACAC ATCTCAGGGG CCCTGCATCC CCAGCGCAGT 1440 GTGCACATGG TTCCCTATGG GTAACTGGCC CCAGCGCAGT GTGCACATGG TTCCTGACGG 1500 GTGACTGGCC CCAGACCCTC TGGCCCCCCA GCAGTGTAAG CAGCTGGGGG CCATGACGCA 1560 GAGGCCCCCT GGGCTTCCGC AAGGATGGAA AGAGCTTGGG TGGAGGGCCC AGGAAGGAGA 1620 CTGTGGGCAT GAGGGCCAGC GCCCTGACCT GAGGGCACTG GACACTGCTT CTGTTCACTG 1680 CTGCCATCAG GAAGGGCTGG GCTGCCGGCT TCTCAGAGGG AGTCAGGAGT GAGATTCTAT 1740 CTGAAATATA CAATTTCCCT CCTGGTCATT AAGGCAAACA AACTAAAATG CCGCAGGGAC 1800 CATGTAGATT GCAGTGGCTG CCCACCCCCA GGGCCACCCA TTTGTGGCCT GAACCATTTA 1860 CCAGCCTTGG AGGTGGCTGG ACCCAGGTGT GGGCTCCCCC TGGCCTCCTG CCCTCTGTTG 1920 GATGCGCTCT GGGGTCGGGA AGGCCGGGGC AGGGTTGCAG GACGGAGGTG GGGGGCCCCC 1980 ACCATGCCCC AGGGGATGAG CCTCTGAGTA CATCAGAGGG GAGAGAGGAG GGGCCAGGCA 2040 GGGAGGAGGG GCCAGGCAGG CAGGGAGCCT CTAAGCACTT GTGGGAGGAG GTGGGGCCAG 2100 GCAGGGAGGG GCCAGTGAGC CACCTCGGAA CTCAAGGTAG TCAACATTCC CCACAGAGGC 2160 GGGGCCCTGG GCTGCCACAG GGCCAAGCTG GGAGGTGATG CCAGGGCCTG CCCCAGAGTC 2220 CAGCCTCTCC TGGGCTGCCA GTTCTCTGCT TTTCACACTG GGGGCCCCAG CAACACAGGG 2280 TCTGACCTCT CGCTCCCTCC 2300
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