Tag | Content |
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EnhancerAtlas ID | HS044-09017 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr3:66101150-66102460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr3:66101263-66101274 | TAATTCAATCA | + | 6.14 | ESRRB | MA0141.3 | chr3:66101423-66101434 | TCAAGGTCATT | + | 6.32 | Esrra | MA0592.2 | chr3:66101422-66101433 | GTCAAGGTCAT | + | 6.32 | Esrrg | MA0643.1 | chr3:66101423-66101433 | TCAAGGTCAT | + | 6.02 | ZNF263 | MA0528.1 | chr3:66101604-66101625 | CCTTTCCTGTCTTCCTCCTCC | - | 6.86 |
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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 |
GH03I066115 | chr3 | 66100892 | 66103212 |
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Enhancer Sequence | GGGTCTCTGG AGTACTGGGG TTTTGTTGGA GTCCCCTGGG ATCCAGGATA TAGCGGGAAA 60 TAGCCAGGAA AGAGGAGGAG CTGAGCTGAT AGAAATACAT GCCCCATCTC CCCTAATTCA 120 ATCAGATTAA CTGCATTTTA TGCTTTTTTT TTTTTTTTTA CATTGTTTCA GAAGCTAGTT 180 ATTTATTGCT CAGAACCCTT CCCTCACTCT TTCTTCCTGA CCCTGATTTT TGTGTGCAGG 240 GAAATGGGCT CAACTTCAAG CTATGGAGTG TGGTCAAGGT CATTCATGAC AATCCTCTTC 300 CTCAGTTTCT CAGTCTCCCT GGAAGCTATG GATTGGCATA TGACCCAGTT TTAGCCCATG 360 AAATGTGAGA ATAAGCCACT TTAGCAGTTG CTGCTAAAGT TTTTAGGAAG CTTTTATTTT 420 CTTACTAAAA AGGGACATAT GTGGCTGATA TGGTCCTTTC CTGTCTTCCT CCTCCCTTCC 480 ATGCTAACAT CATGTCTGCC ACTACAACAG CAATCTTGTG ACCATGTGGC TGTAAGCACA 540 GGAATGCCTG GAATCTCAGA AACATTGGCT CTGACCTCCG TGAGTCACTG AACCAATTCC 600 GGCAACCACC TGGCTCCAGA CTTCTTGCCA TGTGAGGAAG AAGCCACTAT TGTCTAAACC 660 AGTGCAGAGT TTTCTGTCCT TGCGTCTCAA AAAGCATTCC TCACAGATAT ACATATATTG 720 TGCTTCCAGA TAAGATTTTG TTTAGGATTC TGAGTCTAAA AATAATTTGA AATCTGATCT 780 CATACCATCT TTTCATTGTA GAGAGATAAG GTAACAGTTT CAGTTGTCTG TTGCTGCATT 840 ACAAACTATC TCAAAACTCC CTGGCTTAAA ACAATAGCTG TTTTGTTACC TCTTAGAATT 900 CTGTGAGCTG ACTGGGTTCA GCTGGGCAGT TCCTCTGTTC CTTGGGATGT CTGCATTGCC 960 TACAGTTACC ATGAGGCTCA ATGGGCTTGT CTAATGCCTT GACAGGAATA GTCAGAAGGC 1020 TGGGCTCGGC TGGGACACAG GTCCTTTCTC TCTCCTCATG CAGTTTCAGA GCTTCTCTCT 1080 GTCTACATGG CCTCTCCATG TTGACTTCGT ACATGGCACC TTCACGCCCC CAAAAGCAGA 1140 AGCCACCAGG CCTTCCTAAG GCTTAGGCCC AGATCCAGCT TTGTGTAACA TCTGCGGCAT 1200 CCCTTTGGTT AAAATGAGTC AGGTTCAAGG ATAGAGGACT ATCTGAGGGC ATAAATACAA 1260 GAGGTGTGTT TTATGGGAGG CAATCTTTGC AGGTTAGCTA CTACAGAAAC 1310
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