Tag | Content |
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EnhancerAtlas ID | HS007-15128 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr7:2268470-2269610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr7:2268695-2268706 | TAATTCAATTA | + | 6.14 | Phox2b | MA0681.1 | chr7:2268695-2268706 | TAATTCAATTA | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTTCACACCA TTCTCCTGCT CCAGCCTCCC GAGTAGCTGG GACTACAGGT GCCACGCCCA 60 GCTAATTTTT TGTATTTTTA GTAGAGACAG GGTTTCACCG TGTTAGCCAG GATGATCTTG 120 ATCTCCTGAC CTCATGATCC GCCCACCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCCTG 180 AGCCACCACA TCTGGCCACA AGCTAGCATT CTAATAAACA CACATTAATT CAATTATGCA 240 ACAAAACAAA TGCACACGCA CACACAGTTT AACCAAATGC AGCAGGGCCT CATCTGGGCT 300 CTGAGAGCGC AGGAAGCCAG AGCCTCCTCT AATGCGGACA GAACTACAGA ACGGCTCTGG 360 GGACCGCAGC AGGGACTGGG AAAGAGGGTC CAGGCAGAGG AGCCTAGAGG AGCCTGCGCA 420 GCCACAGGGC CCAGGCAAGG CTGGAGACAC TACTAGCCAG CACTCCACTC CCCACCACTC 480 CCTACAACTT GGGGGCCCCA TTATCGCAGC CCCAACTGGG ACTGGGCTCA TCACTCTTTG 540 GAGCCTGAAG TCCTTCAGGA GGCCTGAATC CTCTGCAGTT GTGTCTACAG TGAGAAACCC 600 CAAGAACTTG TAATGAAACA AAATACAACT ATTTTATAGA AGAAAACTGT AAAAATCACC 660 CCAAAATCTG TAAATGGCCC TCCACAGTCT GAGACCACAA AACACCCAGT CCTTCTGCTC 720 ACTGCTGTGG CTTTGTCTCT GGGCTGCCCA GGCACTCTCA GCACTGTGTT TCCAACACAG 780 CCTTCCCGAC AGTCCTGGTG CTCACTCCCC CAGGCAGTTT GGGTTCTGTC CTCAATTAGA 840 TGAATGAACT GGCTTTCCGA TCCTGTCACC AGGGTCTGTG AGTGCACTTG TGTGAACGCA 900 ATGCTGAGCG CCAGGCCCAC TCAGGGCGCT AACAAGGCAG GCCTTTAAGC CAGGATGGCT 960 CAGGGCCCCA ACTAGCCTCC AGCTACGACC CCAAAATGAG GAGTGCCCAT AGTGAGACCT 1020 GGGAGACGAA TAGCTGTCTC TAGGCTCTGC TAATACCGAC CCACCTCAAC TACAGAAGAC 1080 TGGAAGAGGT CCTGCCCGGG CCCAGGGTCT CCCCAGAGCA GACTCCCACC CAGGCACATG 1140
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