Tag | Content |
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EnhancerAtlas ID | HS191-07042 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr11:63569570-63570920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PHOX2A | MA0713.1 | chr11:63570671-63570682 | TAATCTAATTA | + | 6.32 | PROP1 | MA0715.1 | chr11:63570671-63570682 | TAATCTAATTA | + | 6.14 | Phox2b | MA0681.1 | chr11:63570671-63570682 | TAATCTAATTA | + | 6.32 | SP2 | MA0516.2 | chr11:63570184-63570201 | AAGGGGGCGGGGGGGAT | - | 6.01 |
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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 |
GH11I063801 | chr11 | 63569407 | 63572303 |
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Enhancer Sequence | TCTCTCTGTC GCTCAGGCTG GAATGCAGTG TCTCGATCTC GGCTTACTGC AACTTCCGCC 60 TCCTGGGTTC AAGCAGTGAC TCTCCTACCT CAGCCTCCTG AGTAGCTGGG ATTACAGGTG 120 CCCGCCACCA TGCCCAGCTG ATTTTTTTTA CTTTTAGTAA AGACAGGGTT TCACCATGTT 180 CAACACGCTG GTCTCGACCT CCTGACCTCA GGTGATCCGC CCACCTCGGT CTCCCAAAGT 240 GCTGGGATTA CGGGCATGAG CCACCACGCC AGGCCCATAC CTTTTTTTTT TTTTTTTTTT 300 TTGAGACGGA GTCTCACTCT ATCACCCAAG CTGGAGTGCA GTGGTGTGAT CTCAGCTCAC 360 TGCAACCTCT GCCTTCAGGG TTTTAAGCAT TTCTCTCTGC CTCAGCCACC CGAGTAGCTG 420 GGATTACAGG TGCTCACCAC CACGCCCGGC TAATTTTTGT ATTTTTAGTA AAGACAGGGT 480 TTCACCATGT TGGCCAGGCT GGTCTTAAAC TCCTGACCTC AGGTGATCCA CCCACCTAGG 540 CCTCCCAAAG TGCTGGGATT CCAGGTGTGA GCCACTGCAC CCGGCCTGCC AGGCCCATAA 600 AATTAAAAAA AAAAAAGGGG GCGGGGGGGA TTTGGGGAGA GAATGCAGTG TCTGGAGTAT 660 TAGTCAGCTT TTTGTTGTGG CAATGTTGTG TAACCAACAA CCCTGGAACT TAGTCATTTA 720 CGGCAGCAAA CATTTCTTTC TTATAGGTCT GTAGGTCAAC TGTGGCTGCA CTAGGCTAGC 780 TGGGCTCAAC TGTACTTGGC CCAGCTGTAC TGTGAGTTAG GTTCCAGTCT ACTCCAGGTG 840 TCTCTCATTC CAGGACCCAA GCTGAAGAAG CAGCATATCC CTAGGGCATG CTCTTCTCAG 900 ATGGATGGCA CACGCAATAG AAACCAAGCA CACACCATAC AATTACTACA ACGCCTCAGC 960 TAAGATTACT GCTTACTTCA TGTCTGTTCA CGCCCCATTG GCCAAGGCAA GTCACATGGT 1020 CACGTCCACA GTCACAAGGG TGGGGAAACA TTCACTGTCT CATTTGAGGC ACTGAAAAGC 1080 AAGGTAATGG GGCTGGACAT ATAATCTAAT TATAGGAGGG GGTGGGATAG CTGGAAACAA 1140 TAAGCCAACC AACTCAGAAC AAATGCTTGC CATTCTTGCT CTACGAGACC TTTAGGGAGC 1200 AGGTCAAGAA GGATTCATCA GGCCAGGCAT GGTGACTCAC GCTTGTAATC CTAGCACTTT 1260 GGGAAGCCGA GGTGGGAGGA TCACTTGAGC TCAGCAGTTC AAGTGGCAGA ACATGGCAGA 1320 ACCCTGCCTC TACCAAAAAA ATATAAAAAT 1350
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