Tag | Content |
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EnhancerAtlas ID | HS178-01494 |
Organism | Homo sapiens |
Tissue/cell | Skeletal_muscle |
Coordinate | chr1:117026450-117028310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:117028046-117028065 | TGCTGCCACCTGCTGGTCA | - | 8.19 | ESX1 | MA0644.1 | chr1:117027378-117027388 | ACCAATTAAC | + | 6.02 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_27848 | chr1:117025880-117028311 | Fetal_Intestine | SE_28774 | chr1:117025688-117026971 | Fetal_Intestine_Large | SE_41250 | chr1:117025585-117028233 | Left_Ventricle | SE_47846 | chr1:117026072-117026699 | Pancreas | SE_47846 | chr1:117026717-117027069 | Pancreas | SE_47846 | chr1:117027355-117027932 | Pancreas | SE_50584 | chr1:117023434-117028613 | Sigmoid_Colon | SE_52493 | chr1:117023308-117028704 | Small_Intestine |
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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 |
GH01I116481 | chr1 | 117023899 | 117028464 |
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Enhancer Sequence | AGAGCAGGGA AGAAGGATTT GCAAGTTTCT CACACATGCC TTGGCTTAAG CAAAGCTTGC 60 TGGCCTCCTT CAAGCCATAG CACAGGGTGG CGTTTGCCGT GCCTGACTCC CCAAGCTAGG 120 CACTGGGAGT CCAAGTGAAC CATCTGGAGG GGTCAACAGT GACGTGAGCA GATAAGCCAC 180 AGCACATTGA GCTAGAGGAG GAAAGAGGAA TGTGCACATC CCTGCTTGGA TGTGGGGGCA 240 GGAGGGGGAG GGCTCCAGGA AACCTCGCAC AGATTCTTTG GGCTGCCTAA ATCCCGCTGC 300 TCCATGTCTA GGTGGCTGAA GCGCCTCCTG GCCTGCCTCA ACCCCTCCTC TGGCCTGTCC 360 TGTTTACCAG CCCTGCCACC TGCCCACTCT AAGAGGCTCC ACCCTTCCTT GGAACACGGA 420 GTTCTCTGCC TCTGGACTCT GGGGAGGGTG AGATTGTTGA GGCAGGCGGG CGAGCATGAG 480 AGGGAAGGAA GAGGGAGGGA GGTCAAAGAT ACAAGGTGAG CTGGAGAAGA AACGGACTGT 540 TTTGAGGATT TCCCCTCACA CATTCTGGCT CCTACCTCTG ACCGAAAGCA AAGGGAGCAG 600 CTTTTACCAA TGGAATGAGG CCAGGGTGTG TTGGCTTACA CCCATAATCC TAGCACTTTG 660 GGGAGGCCAA GGTAAGAGGA TCAGTTGAGC TCAGGAGTTC AAAACCAGCC TGGGCAAGAT 720 AGCGAGACCC CATCTCTACA AAATTTTTTT TTTAATTGGC AGGCATGGTG GCATGTGCCT 780 GTGGTACTAG CTACTTGGAG GCTGAGGTTT GAGGATCTCT TGAGCCCAGG AGGTCAAGGC 840 TACAGCAAGC CATGATCGTG ACACTGCACT CTAGCCTGGG TGACAGAGTG AGACCCTGCC 900 TCTAAATAAA TTAAATCAAT CAATCAATAC CAATTAACTA ACTAACCAAC CTGTCTATCG 960 GGGTCAGTCA GCTCTTATAG TCCCACCTGA ATTCTGCTTT GCCTTCTCCT GCAACAGCAA 1020 CGCCTTCGAA AGTGCTTACT GTGTGCTAGG CAGGCGTTGC ACATGGACAG GGACTGGGAG 1080 TTCAGATGGC CAGCTGGCCT GCTGTCTGGG GACAGGGGGT TTCCCAGGAC CTGAGACTTT 1140 CAGTACTAAA ACCAGGACAG TCCTGGGCAA GCTGGAACAG CTGGTCACCT GGTGGGAACT 1200 GAGCACCCAT GGAGTCAGCA GAGAAGGAAG GCGGCACCAC AGCATAGCTG GTGGTGGGAG 1260 CAAGCAGGAG TCTTTTCCTC CTTAGCACTG GAAGCGCCAC TCTTGGCATT TACCTCCCTT 1320 CCTGAATGGA GCCCCACCTG TTTTTATGAG GCCTCCCCAG GCCAAGCCCT CAGGATGGGC 1380 AGGGGTGGGT TGAGACTGTG CTGTCTCTGC TGTTTGCTAA GGTTGTTCTC ATGGTATCAC 1440 GCTGCCAGAG ACTGTCCACT TGGCTCACAT TGATGGAGGT CAGCTAAGGA CAGGCTGATT 1500 AGCTGGCCCC TCAGGGCCTT TCTCTTGGTG ACACAGCCTC TGGCTCAGAA CAAAGGCCCC 1560 TCATTTTGCT GAGGCACAGA CTCTTGAACG TGAGAGTGCT GCCACCTGCT GGTCACAGCG 1620 CTGCTTCCAG AAGGGGAGCT GGAGCCTCAG GAGGGAGACT GGGCCATGAG CCCAGGTCTG 1680 TAGCCTCTCT GTGGGCCACA GCACCACCTC CCAGCATGCC CTGGGCCAGA TAGCTGAAGA 1740 AAAGAAGCTG GGGACCCCCC TAACAGGTAT GCCTTGAAGG GGACTGCAAG GCTCTCTCAT 1800 GCCAGAACTC TCTCAGGCTG GCCATGGATT CCCAGAATTC CCAGCCAGCG TGGGCACTCT 1860
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