Tag | Content |
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EnhancerAtlas ID | HS040-00460 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:11402050-11403480 | 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 | GAGAACAGCA AGCCCGAGGC TCCATCTCCT GTTTACCGCT GGCTGTTCTG CTCTGTTTCT 60 GATCCATGGC ATGCAGCCAT GACTTTATAA CTTACAAAAT CCTTTATTGC CATAAGTGGA 120 GAGGAGTTTC ATGCATGCAA ACTTGTCCCA ACCTGGCAGC TTCATCTTCA TTTTGTAAAT 180 GTTGCAATGA AACTCCAGGA GGTTCTGTGC TTGCTGGAGG CGTATGGGCC ATATGGTGTG 240 GAGGAAGGGC TGTAGTTGAC CACTGCTTTA TAAGCAGCTT TGTAAACGTA TATATTTCAA 300 GATGACACAC ACATACACAC ACACACCCCA GTCCCAGAGT GACACAATCA TAGGGCCATT 360 GCCAGAGCAA TCATGAGTAC TGAAAAAGTG AACACATGGC CTCTGCACAC CAGGTCCCAG 420 GCCGCAGCTG TGGCAGACAT CCCTAATCAA TCACAGGACT CCTTCGTGCT GAGCCCAGAT 480 GCAACCTCAG AATCCTGGAA AGCCCATATG GGGTTGATTT ATAAAAGGAA GCATTGGCCA 540 TTTTTGCTGC AGGGGCAAGC TGTCCTGGGG GGCCTTTCCT GGGGGATAGG GAACAGCATT 600 GGCCTAATCT CGGGTCTTGG AACCCTGTTC TTGAACCCTT GGCAGCATTC TCTGCCGGAT 660 TTATAAAGTG ACTGCAGCTC TGGAACATGA GACAAAATTA GTGCAGCCTC AGAGAGCGCT 720 GTCTCGAAAT TGGCTTTCCA GCGAGCGGCT GGGTCTCCTA CTCTCCCCAC AGGTGGGGCT 780 GTTTGAGTCC CTGGTAGGAT TTGTTCCAGC TGCCAGACAT GGATTAGGCT TTTGACTGTT 840 GAACCCAGAC AAGGGGACCA GCTGTTTAAT GAGCTGGAGG AGGAAGTGGC TCCTGAAAGC 900 AAGTCCTTTT CTTGGCTCAG GCATGCAGAT CAGACATGGA ACCAGGAAAG CTGCCTCGCC 960 AAGCTTGGTA ACCAGAGGGA AATGAATGAT AGTGATCTGA CAGGGAAGGA TAAGGACAGG 1020 GGAGAAGAGG GGAGGTGGGG AGAGGAGCAG GAGGGGAGGA GCCAGGAGGG AAATCATGGA 1080 CCAGCCTTTG CCTAGACCCC AGGGCTCTGC TGCAGGCTCC ACTCCTCTTG GCTTCTTTTG 1140 CTATCAGAAT CATTGTGCCT TGGATCCTGG AGATCCCGAG GCATGTAGAT GATCTAGGGG 1200 TAGGCTAGAT ACAGATTTAC ATTGATACCT GGAGACAGGA TAACCTGGGT TCAAATTCCT 1260 GTTCCTCATT GACTTGCCTC CGTTTCCTCA TCTACAAAAT GGGCTTCGTG TTTCCATGAG 1320 CAGGGGCGTA ATGCTCTCAG ACTTCCCCAC CCTGTCACAT TCTGCCATTC AGCTTTTGGT 1380 AGATGTTCAA ACTGCCATTT GGACCTTTAT CCATGGGATT TCAGTGTCTC 1430
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