| Tag | Content |
|---|
EnhancerAtlas ID | HS040-01662 | Organism | Homo sapiens | Tissue/cell | Esophagus | Coordinate | chr1:53738370-53739540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PRDM1 | MA0508.2 | chr1:53739405-53739415 | TCACTTTCAC | + | 6.02 | | ZNF263 | MA0528.1 | chr1:53738648-53738669 | GGGGGAAGGGGAAAGGAGAGA | + | 6.01 | | ZNF263 | MA0528.1 | chr1:53738858-53738879 | AGAGGAGGGGGATGGGGTAGA | + | 6.59 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGCCCAGC CCTGGGAAGC CTCAGACCCT TGGAGGTGGG CTGAGCCACG GCAGCTCCCA 60
CCTCTAGGAA TCTTTCAGTC GCTCGGAGCC CTCCCTGACC TCTCCTTTCC TGTGTTATTC 120
CCTGAGCACC GTTCATTCAT CTGTCCTCCC ACTCACCCAC TGCCCCCATC ATGCATCCAC 180
TCGCCTCCTT CCTCTCCTTT TGCAGCTAGC AACAACTCAA CAATTCTATT TACTGAGCAC 240
TTGATGAAGT GGCATGTGTA GGTGGGATGG CCCTGAAAGG GGGAAGGGGA AAGGAGAGAA 300
CTCAAAGTGA CTGGCTTCTG ATGAAGGAAG GCACAGAGTC CTCCAGGGCT CAGGTGGGTG 360
AGGGGAAGAG AAAGGAGAGC AGGTCTGCAC CTGTCTGTCC CTGTAACCTT TCCCCAAATG 420
CCTGCAGGGA AGTCTTCAGT CCTTCTTAAT TCTACCTAGC CTGGGTGTGA TTCCGCTGGG 480
GAGCCAGGAG AGGAGGGGGA TGGGGTAGAG TGGTGCAGAG AGGCCAGAGT AGTATTTGCG 540
GCTTCCTTCC ATGGAAGGAA GAAGTGGTGT CACTGCACAC ACCTACATGC ACACACCAGC 600
ATGCCCACAA CTACATGCAC ACATACCAGC TTATGTGCAG AGCACAAACA GTCCCATGGA 660
CTCCATAGAT ACATTCACAC ATACATGGGG TCACACACAT AGATGCATGA ATGCAGTTCC 720
CCTGCTTTAC TCAGAGAAGA AGACATGGAT ACAGACACCG GCCTCTCACC AACACAGAGA 780
CAGAGGCCAC ACACAGACAC AAGCACGTGT GTACGTACTC CTCTTTGGTG TGTCATGCAA 840
ACGACGAGAG AGAAGAGAGG GATTAGTAGG ACAGTAGTCC CTGGCTACTC CAAATCTGGG 900
TGTTGGGGGA GCTAGGCTCA GTAGTTCTGG CTTCCCTGTC TCTTTTTCCA CAAGTTCCTT 960
CTTCTGGGAC TTCTCTTGGC AGGGCCTGGA GGCAGAGGGA GTGTCTATCT CCTGCCAGCT 1020
CAGGTAGAAG CTGAGTCACT TTCACTCAAC TACTCTTCCT TTCACAATCA GTTTTTTAAT 1080
CTTCAAAAGG GGAAGGAAAT ATGCTCTTCC TGGGAAGCTC AGGAGGATGA ACCTCCTCTA 1140
AGCACCCAGG AGGTAGGTGC TGGGGAAACA 1170
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