Tag | Content |
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EnhancerAtlas ID | HS044-00072 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr1:11402120-11403320 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr1:11402277-11402287 | GCCATATGGT | + | 6.02 | ZNF263 | MA0528.1 | chr1:11403090-11403111 | AGAGGAGCAGGAGGGGAGGAG | + | 6.58 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGCAGCCAT GACTTTATAA CTTACAAAAT CCTTTATTGC CATAAGTGGA GAGGAGTTTC 60 ATGCATGCAA ACTTGTCCCA ACCTGGCAGC TTCATCTTCA TTTTGTAAAT GTTGCAATGA 120 AACTCCAGGA GGTTCTGTGC TTGCTGGAGG CGTATGGGCC ATATGGTGTG GAGGAAGGGC 180 TGTAGTTGAC CACTGCTTTA TAAGCAGCTT TGTAAACGTA TATATTTCAA GATGACACAC 240 ACATACACAC ACACACCCCA GTCCCAGAGT GACACAATCA TAGGGCCATT GCCAGAGCAA 300 TCATGAGTAC TGAAAAAGTG AACACATGGC CTCTGCACAC CAGGTCCCAG GCCGCAGCTG 360 TGGCAGACAT CCCTAATCAA TCACAGGACT CCTTCGTGCT GAGCCCAGAT GCAACCTCAG 420 AATCCTGGAA AGCCCATATG GGGTTGATTT ATAAAAGGAA GCATTGGCCA TTTTTGCTGC 480 AGGGGCAAGC TGTCCTGGGG GGCCTTTCCT GGGGGATAGG GAACAGCATT GGCCTAATCT 540 CGGGTCTTGG AACCCTGTTC TTGAACCCTT GGCAGCATTC TCTGCCGGAT TTATAAAGTG 600 ACTGCAGCTC TGGAACATGA GACAAAATTA GTGCAGCCTC AGAGAGCGCT GTCTCGAAAT 660 TGGCTTTCCA GCGAGCGGCT GGGTCTCCTA CTCTCCCCAC AGGTGGGGCT GTTTGAGTCC 720 CTGGTAGGAT TTGTTCCAGC TGCCAGACAT GGATTAGGCT TTTGACTGTT GAACCCAGAC 780 AAGGGGACCA GCTGTTTAAT GAGCTGGAGG AGGAAGTGGC TCCTGAAAGC AAGTCCTTTT 840 CTTGGCTCAG GCATGCAGAT CAGACATGGA ACCAGGAAAG CTGCCTCGCC AAGCTTGGTA 900 ACCAGAGGGA AATGAATGAT AGTGATCTGA CAGGGAAGGA TAAGGACAGG GGAGAAGAGG 960 GGAGGTGGGG AGAGGAGCAG GAGGGGAGGA GCCAGGAGGG AAATCATGGA CCAGCCTTTG 1020 CCTAGACCCC AGGGCTCTGC TGCAGGCTCC ACTCCTCTTG GCTTCTTTTG CTATCAGAAT 1080 CATTGTGCCT TGGATCCTGG AGATCCCGAG GCATGTAGAT GATCTAGGGG TAGGCTAGAT 1140 ACAGATTTAC ATTGATACCT GGAGACAGGA TAACCTGGGT TCAAATTCCT GTTCCTCATT 1200
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