Tag | Content |
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EnhancerAtlas ID | HS050-59224 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr6:90694730-90696130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr6:90695704-90695716 | GCCCACGTGCTC | + | 6.27 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_37285 | chr6:90694002-90701235 | HSMMtube | SE_51961 | chr6:90694451-90697519 | Skeletal_Muscle_Myoblast | SE_63743 | chr6:90694325-90697592 | HSMM |
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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 |
GH06I089984 | chr6 | 90694375 | 90698440 |
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Enhancer Sequence | TCGGGCAGGA GACATTTGGC CGTGCCTTTC CTATTTTCCA GGGATAGGAC TGTGAGTTAC 60 TTCCGTGTGG TGGGCGGTGG GTGCTTGCAG GGGTGAAGTA CTAACAGGTA GCAAAGTGTT 120 GGAGACACGA AGCATTAATC ATCAGTCAAC AACAGCAGTG GCAGCACTGC TATCTTTCCT 180 GGGGCTAGTG AGAATTAACG GATTAATGTT TAGGAGAGCA CAGAAGTTTC CAAGCATCTA 240 CTGTGGTTCT CAATCCTTTG CAGGGAAGTA AACAACTGAG GTGGCCACCT GGGATTCTCA 300 TCTGCTGGCG GGGCTGGTGG GAGTCTGGGT TTTGTGGGTG GCCTCAGGGG GCCCTGGCGG 360 CAGCTTCCAG CCTCTGTGGT GACAGGCCAT CTCCTCTCTG TCTAGTTCAC AACTCCAGAT 420 GCTGTGGGGA GGTGGCAGCA GTCCAGTGGG GGCGGGACAC TAAGATTCTC ACATTAACAA 480 TGCACAGACA TCCGTCCATC CGGCACTCCT GGGTCATGTC CCTGAGAGTG ACACAGGGCT 540 GCCCCTGGGG CAGACACATG AGATCATCTG AACTGGTTAG CTCCAGAGGG CCTCAGCTGG 600 GCAGGGGCTC TGCAGCTTTT GTCAGAGGCT GTTTCCCTGC AAAATGGGGG GAAAATCGGA 660 ATACTCAAAC AAAGGGGATT TCTGTAACTC TTCTGCCATT TTTCTCTCAC CTTTTCTGTG 720 TAGCTGAGCT CTTAGGAAAC TGGTGTTAAA GCAGTTCAGT GAGAAGCAAG GCAACTGAAA 780 GCCCCTTCCA ACAGCTGCCA ATGGTTGTGG ACGAGCAGGC AGACACCAGG GCTAGGAGGA 840 AGGGAGCCAA CAATCACTCC ACAGTGGCAT TTTTCAGGAC TCAGTCATTT CTGATGCTGG 900 AAAGAAGCTT GAGAAACCAA AGTACAGCTG TGGGAAGACA GTGTGGGGCT GGAGGGATGC 960 GGGTGTGGGC TGCTGCCCAC GTGCTCCCTG GCCCTGTTAT AGCCGGACTT GTAAGGCTTT 1020 CTTAAGCCTT GCATCTGAGA AAGGCAGAGA CCAGAGAATG GAAAGACAAA GCTGGGGAGA 1080 CTGATAGTGG CGGCGGCGAA CTGAACTCAG CCCCCTGCCT GTGGAGGGGA TGGGCTGTTA 1140 GTGCCTGGGC CATGGATGGG GGAGCTCTGT AAGGATGGCT TTTTTCGGTA TGTGTGTTAA 1200 AGTCTGAGTT TTTTTTTTTT TTTTCCTGTG GGGTTTACAA GCTCATTCCA TTGTCCAGAA 1260 TCCTTGTGGG CATATTTCTC CTAGGGACGC TGGCCCTGGA TCGCTGGCCT TGCCTGAAAG 1320 AGGCTGCCTC CTACTGCGTT TTTGTTCAAC TTGCTTTCTC TGTAATAGAG ATTTGCAGCA 1380 CTGTGGGCTT CAGGGATTCA 1400
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