Tag | Content |
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EnhancerAtlas ID | HS139-33363 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr20:46092730-46094120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr20:46093950-46093962 | ACATCAATCAAA | + | 6.74 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_35639 | chr20:46092648-46094153 | HepG2 | SE_43387 | chr20:46090929-46096523 | MCF-7 | SE_58317 | chr20:46012297-46142322 | Ly1 | SE_60400 | chr20:46012252-46151621 | DHL6 |
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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 |
GH20I047463 | chr20 | 46091881 | 46094944 |
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Enhancer Sequence | CCTTGAACAA GGGAGGCGGA GGTTGCAGTG AGCCAAGATC ATGCCTCTGC ACTCCAGCCT 60 GGGTGACAGA GCGAGACTCT GTTTCAAAAA AGAAAAAAAA GAGTTCATTC TGTATGATTC 120 CATTTATGTG GAGTCTAAGA ATAGAGAAAA CTAAGGGTGA TAAAGGTCAG GATAGTGGTT 180 ATCTTGTTTT GGGAAGGGGC AAGAGGGAAC TTTCTGGGGG ATGGAAATGT TCTGTGTCCT 240 AGGGGATGTT TGGCACTGTC TGGAGAGGTT TTTGATTGTC ACAACTGGTG GTGGGGGTGC 300 TACTGGCATT TAGTGGGTAG AGGCCAGAGA TGCTGCTAAA CTGAATCTTA CAATGCACAG 360 GATTACCCCA AAACAATTAT CTGGCCGGAA ATGTCAATCG GGCTGAGAGT GAGAAATTTT 420 GGTATATGAT TTAAATTGCT TAAACACGAT CAAGGCATTT CTGCATCCTT GTGGGCATTT 480 GCCATTACTA CAGGCAATAT TTGAGTGACG GAGACGGCTA GTTATCCTTA GGATATAGAG 540 TTGTCATTGG AAAGCAGCCA GGGACAATAT TTCCCAATCC CCTTTGCATC TGGGTACAGC 600 CTGTGATTCA TTCTGCAAAT AGAATGTGAG CAAAAGCAAT GTGTATTAGC TCTGCACAAA 660 GCAGTTGAGA AACATGTGCG CCTTTTCCAT TCTCCTTCCC CTGCCACCAC TGGATGCAGA 720 CATCAACGAT GAGGCCCCAG GGATGGAGGA AAGCTGTCAG TCAACTGGCA ATGCAGCGCT 780 AGAGGAGATA AACTTCTATT ATGCAAGCCT CTGAAATGTG AGCGTTATTT GTTACAGTGG 840 CTAGCGTTAC TCTAATAGAG TATTCAACAA AAAAAATATA GTCTTTGAAG GGCAGGTCTC 900 CCAAACTGAT ATATTAAGGG GCAGTTAATC TCACTTGTAA ATTCTCTGAG AGCAGGGATC 960 ATGTGCTACA CATTTTCTTA ATCTTCGATA ATGCTAAGTA CCATGTTGAG CAAATGACAT 1020 GTTTCTTTCT CTCTCCTTCC ACCCCCGCCC CCAAAGTCCT ATGACTTCCT GGGTTGGAAG 1080 AGAATGTAAG TGTTCTTTTG TAATCTTTCC AGGACACCAT TAATGGAACC ACAGAACACC 1140 AACTTTCACA CTCTAATTCC ATGTGTTTTG GAATAAGATT TACTTTGCCC CATGCTCCAG 1200 AGTTGGGTCC TGATTGGCTT ACATCAATCA AAGTCTTTTC TTTACCCTGG CCTTCCCACT 1260 CTGTCACCCA GGTTGGAGTG GCACAATCTC GGCTCACTGC AACCTCTGCC TCCTAGGTTC 1320 AAGTGATTCT CCTGCTTCAG CCTCCTGAGT AGCTGGGATT ACAGGCACAT GCCACCACGC 1380 CAGGCTAATT 1390
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