Tag | Content |
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EnhancerAtlas ID | HS139-37875 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr3:99690960-99691980 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TBX20 | MA0689.1 | chr3:99691797-99691808 | CTTCACACCTT | - | 6.32 | TBX21 | MA0690.1 | chr3:99691798-99691808 | TTCACACCTT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_02061 | chr3:99691126-99691964 | Aorta |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I099972 | chr3 | 99691127 | 99691964 |
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Enhancer Sequence | TATTGCAGAC ATATAAAAAT ATAGACTGAT ATGCAAAGTG TGGGGAAAGA TGTCATTCAA 60 ACCAGTCTTT TTATGGGCTT AATAAATTTG ATAAGGGAAT AGGAAGAAAG CTAGTCATCT 120 CTTTCCCTTA GGTTGAAATA AACTTGACCC AATAGAGTAC CCTAGTTTTG TTCATTTGCC 180 GAATTGACTT AGATGCCAGG GATTTGCATG TGGAAAACTA ATGCCATGGC AGGATTACTA 240 GACTGTAAAT TCATTAAGAA GTCTGATGAT ATCATAAACC GTGAGAAGCC TCTGTCTTGC 300 AGCAGCATCG GAAACGTCCC CGTCCCCATT TGAGTAAGTG CTGGTAATCC ATTTTATTTC 360 TCTCCATTAG TTATTATAAT AATAACAGAT TGGTGACACG GCCTCATTTT CTGCCTCTAG 420 TGCTGTCTGC TGCTGGGCAC AGCTGCTCCC AGTCATTCTT TCCAGAGTAA ATAACGGTTC 480 ATGTTTCCAT GGGCTGTCGC GAGAGCTTTC TGTGCTTATG AAATGAGCCC ATGTCACCAC 540 CCTGTTGGGA AAGATTGAAG GCATGGGCAA AGCCAAGGAA CTGCATGGGA AAGCCAGAGC 600 TTTACCCCTA CCCTAAGATA TGTTTTTTGC TCTTGAAGAC ATTTAGATTA ACTGGGTGTT 660 AATGATGTTA ACTTCCATAA GTGTGAGGCA AGAAAATTCC ATCACTTGGC ATCTGTCTGA 720 TGCAGGCCTT TGGCTTTGGA ACTTTTTCTT TCATGTTAGA TGTAAATAAT GAACTCCTTT 780 GTTGTGAGAG GGTTTGTTAC AAGGAAGTAA ACACATCAGC AAAGAGCATC TTTTGATCTT 840 CACACCTTTG GCAATAAAAG CTGAGAGCAG AAATAGGCCA GAGAATTTGG GACAGAAACC 900 ACTAAAAGCT CCCCTTTTAT CTGTTCACAA AATTAGGTGC AGAACTATAG GAACAATGGA 960 TGGAATGACA ATTATTAAAA AAGATGAAGG GCAAAATGAG GCCACCTGAA TAATAAAAGC 1020
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