Tag | Content |
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EnhancerAtlas ID | HS044-10690 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:133575710-133576950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr5:133576431-133576446 | TTCTATTTTGGGCTC | - | 6.1 | ZNF263 | MA0528.1 | chr5:133576208-133576229 | GAAGGAGGGAGTGAGGGGGGC | + | 6.54 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_41285 | chr5:133575404-133577132 | Left_Ventricle | SE_51500 | chr5:133575112-133578985 | Skeletal_Muscle |
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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 |
GH05I134239 | chr5 | 133575635 | 133578526 |
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Enhancer Sequence | GGCAACTGCA TTGTTTCTAG GATTTAGTTC TTGCGCACGC TGCTATTATG AACATTATTG 60 TCAATGTCTC CTGTTGTACC CGTGCAAGCA TTTCTCTAGA AAATCAATTG ACGCTTCCCC 120 CAGCCATGGA TGAGAGAGCC TCTGGATCCA TATCCTCTGG TATTGATGTT TCCATGGTTT 180 GGGATCTATG TTGTCAAGTT GCTTTCCAGG TGGTTAGATC AGTTTGCCTC TCCTCCAGCA 240 ATGCAGGAGA ATGCCCATTG CCCCAAACTC CTTCCAACAC TGGGAATCTT TAAAAGATTT 300 TTGACCATTT CATAGGAGAA AGATAACATC TCCCTGCTGT TTAACTTTGT GGTAAGGTAC 360 TGACTGTTTC AGAAGCTGAG CGAGAAGGGA TTTGGTTCAG AGAATCGTTC CCAGTCTGAT 420 AATTTCAGTG ATATTTCTGG AACTGATTAC CCAGTGGCTC AGATGCTTTC CCATGTCCTG 480 AAAGAGGTGA CACTGTTGGA AGGAGGGAGT GAGGGGGGCC AGGATGGGAA ACAAGCCCAA 540 TCACCACAGT GCAAGCTTGT CTTCTGGTCC CAGCCCCTGC CAATGTCAGA TCACTTTTTC 600 TCCTAATGAA ATAGGCATTA TCTCCCCCTA CTCCCCACCC GAGAAAAGCC AGTATAATTC 660 TACCCTTTGT TATTTGAATT GATAAATTTA AACCTCCTTC CCTCTCTGCA GTAAAAGAAC 720 TTTCTATTTT GGGCTCGGTG ACATAGCCAA CACCAAGCAG AGAGCAGCAG GCTGCAGCAT 780 GAGTTAATAG TTTTTCTTCA AGGGAGAGCG AATCCATAAG CAAACAGAAG GCCCTTCCAA 840 ACTGTGTCGT CTGCATAGCA ACATGCAGCC CATTCGCCTG TCTTTATGCT GACGAATATA 900 TTTCTGAAAG GCTGAAAATT GAATACTACC TAATCTTCAG AGGAAGCTGG TGCATTAATT 960 CTGAATTAAT CAGGTTTCTT AATTCCAATC AATTTCCCTC CTCCCCACCC TGTGTACCTA 1020 ACACTGGAAT AGGTACTGTC AGGGAAGGGA ATTCTGTTTT CAAGTGGATT TCTAGTCACC 1080 AAAGATTTAA GGAGTGCCCA AAACATTTTT CCTAAGAATA TGACTTTCTC TGCTAGTCTG 1140 TTTCCATGCA TGAAATCCCC CATATTGGGG TAGAATCCTG GGTCTTACAA GCCCCCAGGC 1200 ATGCATAGAG GCATGTTCAG TTTTTCTTAT GGGAAGTTTT 1240
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