Tag | Content |
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EnhancerAtlas ID | HS060-04817 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:121154510-121155650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr10:121154608-121154622 | TGACCTTGGACCTT | - | 6.24 | SPIC | MA0687.1 | chr10:121155004-121155018 | TCCTTCCTCTTTTG | - | 6.03 | TBX20 | MA0689.1 | chr10:121154911-121154922 | GAGGTGTGAAG | + | 6.02 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_29836 | chr10:121154595-121155758 | Fetal_Muscle | SE_40677 | chr10:121153900-121155858 | Left_Ventricle | SE_43096 | chr10:121153952-121157571 | Lung | SE_48573 | chr10:121153326-121156215 | Right_Atrium | SE_50622 | chr10:121152263-121157313 | Sigmoid_Colon | SE_52928 | chr10:121152274-121156826 | Small_Intestine | SE_54027 | chr10:121153871-121157111 | Spleen |
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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 |
GH10I119394 | chr10 | 121153514 | 121156843 |
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Enhancer Sequence | GCTCATCTTG ATGTGGAAGA GGAGTTGACC TCTGGGGAGA GGCTCTGCCC ACGCGGCGCA 60 GTGGGAATCC AGAGGCCAGC GCGCCAGTCC AGCAGCTGTG ACCTTGGACC TTGGGCAAGT 120 CCCTGACTTC TCTGAGCCTC TGTGTCCAGC CCTATAAAAT GAGGGGTGGG ATTCCTTACA 180 GAACCACTGC CCTATCTCCC TGTGATCTAA ATGATTGTAG TGTTCATGTT TCTTCATGGG 240 AGAAAATCAT TGGATCTTGG CTCTCCATTA GAAGAGAGAG GGCAAGACAA GGACACTCGC 300 TCACTGTGGT TGGAAACGAG CCTGGCTGCC TCTGTGGTCA CTGCGAGTGC CGCCTGCGTG 360 CTCCCTTTGG CTGGCCTGGG AGGAATCGGA CCCTAGACAC TGAGGTGTGA AGTTTCCCTG 420 AGGGCCGGCT GGGCATCTGA CTGCATGGTG GGACGCCTGG GGAGGAGTTC GGGTCCGTCT 480 ATGCTGGTGT CATTTCCTTC CTCTTTTGAA ATAGCTGTAC TTTTGGACAG AGGCTGACAA 540 ATCCTTGGGT GGTGGATTTT GAAATGGTTA TAAACAATTT GCAATTAGCT CTTTTGTCTA 600 AATGAGAAAG GGCCGCTTAC TCAGGCTTTT TATTGACTCG AGGCCCTTTA TCCATGTGGC 660 GAGTGCGTCA GATGTGAGCG AAGGAGCCCC TCTGGGATTC AGGGAAATTA AAAAGTCTGT 720 TTTTTGGAGA CCTCCCATCT TTAGAGCTTG GGCCCCCTGG CTTGGCTAGT TATCAGAGTC 780 CTAAATTCTG TGGTGTGGTT GAGGAGAAGC CCTGCGCTTG GAGGTTCGAG TCCCAGCCCT 840 GCCACCTCCC GCTGCATGAC CCTATGCAAG TCCCTTCCCA CCGCCGGCCC TCGGGATCTC 900 CACCTACAGA CGAGGGGTTG GGATGGCAGC CCCTGTTCTC CTGCGTCACT GCCCTGGCTC 960 TTTCGAGGTT CAGATAAGAA CATCTTAAAA AACCTGTGTA TGTTCACTTT GTAAACTGAA 1020 AAGCTGGAAA AGACCAGGCA TCCACATTAT TGTTTATCCT TGCAAGGTGT AATAATCACA 1080 ATGGCGGTAA CTATAGCAAC TGTTTATTAT TATTTATGAT GGGCCAGGCC CCAGGCCAAG 1140
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