Tag | Content |
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EnhancerAtlas ID | HS139-17627 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr14:102721500-102722600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr14:102722303-102722318 | CTGTGACTCAGCACT | + | 6.47 | Nfe2l2 | MA0150.2 | chr14:102722301-102722316 | CACTGTGACTCAGCA | + | 7.26 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_45661 | chr14:102721339-102722793 | Osteoblasts |
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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 |
GH14I102254 | chr14 | 102720636 | 102723732 |
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Enhancer Sequence | AAAAATTAGC CAGGCGTGGC GGCAGGCGCC TTCAATCCCA GCTACTTGGG AGGCTGAGGC 60 AGGAGAATGG TGTGAACCTG GGAGGCGGAG CTTGCAGTGA GCTGAGATCG TGCCACTGTA 120 CTCCAGCCTG GGTGACACAG TGAGACTCTG TCTCAAAAAA CAATAAAATA AAATTTAAAA 180 AAAAAGCAGA TTTCAAGGCC TGAACCTAGA CCTAATGGAG CCACAAACGG GCATGCGGGC 240 CAGGAATCTG TGCTTCTCAG ATGCCTTCAG TCCCAGGTAA GAGTCCTCTT CAGGTGCCCA 300 CCCTTCCTTG CCTCCCTGGG TCTCCTCCTG GAAACTCCCT ATTCACAGCC CTAGGGGTAG 360 GGAGCCGTCC TGGTCCCGGG CCAGTAGTTG GGGGTGTTAC TGCTGGCATG AGGTATCAGA 420 GCAACAGTGT GGGCCCAGTA GTCTGAAGTG CTGGAGACCA CACCCTTGCA AAGGAAAGCA 480 CTGCCTAGCC ACTCTCCATA AGCTTCTCCA GAACAAACTT TCCGGGCCCA AGACTATCTG 540 GTTCCCATCA GATTCTTGTT TTCAAACAGT TTGAAACAAG TAAAATAGAG TACAATTAAC 600 GAGTTACTCA GAAGTTTCTT ATATGCCCCT TAGTGAATTC CAGCAGGCCC CAAAAGCATT 660 TCCCTCATCT GCTCTAGCTA TCCTGACCAA GGTAATTTTT ACAAGTTAAT TTTTACCAAA 720 TATTCTCATT AAGAAGGAAT GTCATATATG ATACTAATAA TTTTAAAAAC TTAAGTGAAC 780 ACAGTGATAA ACCAAGGCAT TCACTGTGAC TCAGCACTAA CTGAAGGAAT ACAGCTGCCA 840 CTGTAGCCTG CAGAATGACG GCATCCCCAG CACACGCCCC TCCAGCGAGG GTGGAGAGAA 900 CTACGAACTA GCCATTCATT AAGGCAAATG AGTTATTATT ATTTTTTTTT TTTGAGACAG 960 GGTCTCACTC TGTTGCCCAG GCTGGAGTGC AGTGGTACAA TCAGCTCATT GCAGCCTCGA 1020 CCTCCTGGGC TCAAGCCATC CTCCCACCTC AGCCTCCTGA GTAGTTGGGT CTACAGGCGT 1080 GTGCCACCAC ACCCGGATGC 1100
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