Tag | Content |
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EnhancerAtlas ID | HS060-01129 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr1:44034190-44035260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:44034665-44034680 | TAGGTCAAGGTCAGG | + | 6.5 | Nr5a2 | MA0505.1 | chr1:44034636-44034651 | AAGCTCAAGGTCAAG | + | 6.65 | ZNF740 | MA0753.2 | chr1:44034890-44034903 | CCCCCCCCCCCAC | + | 6.92 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_05040 | chr1:44033899-44037467 | Brain_Cingulate_Gyrus | SE_05962 | chr1:44033964-44040045 | Brain_Hippocampus_Middle | SE_07193 | chr1:44033994-44036319 | Brain_Hippocampus_Middle_150 | SE_08033 | chr1:44033754-44036540 | Brain_Inferior_Temporal_Lobe | SE_27645 | chr1:44033835-44036299 | Fetal_Intestine | SE_28595 | chr1:44033824-44036285 | Fetal_Intestine_Large | SE_33537 | chr1:44033846-44034858 | H2171 | SE_41575 | chr1:44034184-44034888 | LNCaP |
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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 |
GH01I043568 | chr1 | 44034002 | 44036016 |
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Enhancer Sequence | GCCTTACCAT CAAGGTGGGC ACTTGAACCC TGTGTACAGA TAAAGGAGAC AAAGAATGAG 60 TAACATGCCA GGCCCTAAAG CTAGTTCGTG GTGAACGTGG GAGTCCCATT TGATCTATAC 120 TAGTCCTGAG CCTGTCCTGG ACTTGTGCTT CCAAGGGGTG GAGAGTAGAT AGCCTTGCCC 180 TGCAGCCCCT CGGGGCTGAT ATGGGAGCCC ATGTACAGTG GGAGTGGGTT TGCTGCTGAC 240 ATCTGTTCCT CTTACTCTAT GCTAGTGACT CCTCTGTGTG CCGCCAACCC CTAGCAAGCT 300 GGGAGAAGGC AGCCAGGAGG GAGTTTTTTC TCCCCCTACC AACTTTTTGT GTCTTTAGAG 360 CTTTTTTATC TCCTTTGCCT CCACACACTC AGGCATGGTC TGCAGCCCTG ACCGTGACTC 420 CCAGGGTCAG GACTAAGTGA GGGAGAAAGC TCAAGGTCAA GGCTGCAGTA ACGAATAGGT 480 CAAGGTCAGG ATCGGAGTTA GAAGGGGATC ATTGGTAGGG CTGGGGGTGC CCCGGGTCAG 540 GGCTAGAGAC CAGGCGGTGA CCTGGGGCTC TGCCATGTGA TAGAGCTGAA GGCTGGATGA 600 AGGGAACACT GTGTGTGCGG ACAGGGGAGA GGGGGCTGGA CAGCACAGAG GCCTTCAGGC 660 TGAGCTGTGG CTGTTGGATG CTGCGCGAGC TCCCTGCTAG CCCCCCCCCC CACCCCCTGC 720 AGCCCCAGCA TTCATGCAGT GCTTTCTGCT GTGACCAGCA GAGCATTGAT TCTCGTTCTT 780 CTCAGGGCCT GGAGAGATAA GTGCTGACGC CTTCAGTCTG AGGCGTTGCC TCTCAGACCT 840 GGAAACTCCC TGACAGGGCA GGGGTGGGCC CCACTGCAGC CTCTGCCCTG CCAAAGAGAC 900 TTAGGACCCT GGTTCCTCAA ATCGGGGTAT GCTTCATGCT TAGAAGTCAA GGAAAGGGGA 960 GGGGAGTCTT GAGGGCCCTG GCCAACCTGC AGTTGGGGAG GTTACCCCCA GAGGGGTCAT 1020 AGGGGGCAGG CAGAGCCAGC CCTAATACAC ACATTGCTGT TTGTCTGCAG 1070
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