Tag | Content |
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EnhancerAtlas ID | HS191-20749 | Organism | Homo sapiens | Tissue/cell | Trophoblast | Coordinate | chr2:74966840-74968770 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr2:74968403-74968414 | AGCCTCAGGCA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I074739 | chr2 | 74966347 | 74969939 |
| Enhancer Sequence | CATTTTAACC TTTTGTGGAG CCATTCCCCA TCAGACAATC CTTTGCTGCC ACTGCCAGAG 60 ATAACACCAG GTAGGATGTG GCAATCCAGA TCTTTTCATC TGGATGTCAG CAACAGCAAG 120 GCAGGGGCCT GGACAGGATT CAGGTCACAC AGTGTCTAGC TGGCTGGTGG AGCTTTGAGG 180 TCTTTATAGA GAAGCTCTGC ACTGAGATTA TCATGAAGCC TGTGAGTGTT GGGGGTCAGC 240 CTGAAGGCAG CATTCTCTGA GTGCTTCCAG CGGGAACTCC CTGTCGTTCG TGAAGGCAGC 300 CGTGCTTCTA ACACTGGAGT AGCAGCTACC ACTTGTGAGC ACTTACTGCA TGCCAGGCAC 360 TGTGACAGGC ACCTCTGACA AATTATTTCA ATGATTTCAC AACAGCACTA CTGTTTTTAT 420 CCCCATTTCA CAGATGAGGT GACTGAGACT CAAATAGATG CTCAAAGTCA CTGAGCTAGG 480 AAGTGTCAGA CACAACCACA TCCATGTGGA CAGACTCCAG AGCTGGAGAT TCGACCTGAA 540 TCCAAATACT GTTCTCCCCA GAACTCCAGT TGTGAGACTT TTAAGTGGAG CTTGGAGATT 600 AAGGAACAAC CCTTTTGGGG TCATTCTTGC TAGGGCTGTA TGAAGACAGC AGGTGCACGC 660 AGGCTACTGT GAAGTGCGGA ACCACTTGGC TGGCAGCCTG GAATATAGAG GGGCAATCTT 720 CTCAATGGGT TGTCAGGGCT ACCACATTTT GGACTTGCTG CCAGGAGACC CAGGTTCAAG 780 TCCCCACTCT GCTGCTATCT CACATTGTGA CCTTGAGTGG TCACTAATCT CTCACTAGAT 840 ACTGGGCCTC GGTAGCCTCG TCTGTTAAAG GGGATGACTC AACTTGGGTA AGTCTAAAGT 900 TTTCTCAGCT TTAAAACGCA GGGATTCCAT GTGTCACCTC TCCCAGGAAT ATTTGTATCT 960 GTGGAATGAA AGACCTTTTG CTGCTGTCTC AGAGAAGTAT TTATGCAGGT CAGGGGTCCT 1020 TTCCCAATGC GTTGGACTCA TCCATCTGGA GGAGCTCTTC TACCGAAGGG CACTACCTTC 1080 TCACCAGGCT GTGGCAGCAG AGGGGTTAAA CAGCATGCCC TGCCCTGCTC CAGGCAGAAG 1140 GGTTGTAGGA CTTAATCACG TTTCAGCTTG GCTGTCGGGC TGTGAGTCAC GGTTGCACTG 1200 CGATTATGTA AGCACGCAGG AATAGGTGGC ATGACATATA TGCTGCCAGC AGCCACGGGC 1260 CTCGCCCTTC CGAGTCACCA CTACTTTTTA AGCCTTTTTT TGGATACAAG TTTCTTTGGG 1320 TTCATCTTTG GAATGGAAAT GGAAGCATGA TTGCAGAATA GGCAGAACAG GAATTATCCA 1380 TCAATCAGAG AGAACCCAGC CCTTTAAGAG AAGCTGGAAT TAGAATATGG AATTCCTGAG 1440 CCTTGAGCTG GCATAGCCGA GCCCTGGTTT ATGCTCTTCC TGCCTCCCTC CTTTTTTCCC 1500 TCCTGCCTGT GTGCTCCACT TCCTCTCCTG AGACTCCCCC AAGGTAGCAT CACTCCCACC 1560 AGGAGCCTCA GGCAGGAAAA ATAAGGCCCA GAGAAGGGAC TGTCCCTGGG GACGTGCACT 1620 GAGTGTGTGT GAGGGTGCGG GGCAGGAATA GGAGTGCCAG GAGTCTACCT CTGGAGCAAT 1680 GCCTCCCACA GTATTTCTGT AGGGGAAAGG ATAGAAACTC ACTTCTTGGG TTCCTCCAAT 1740 CACCATGCAC ATGTCAGTCC TTCAGCTATA AATGCAAAGG AAAGCCAGAA CTGAGATTTG 1800 AGCTTTCTCA CCATCTCCAT GGTCAGATAT CTCCACTGCC AAAGGGTTCA TTCCGCCTCT 1860 GGGTTTATCT CTTTCTTCAT GCTTCTTCCT GGCAGTGTCC TGTTGAAGCT TACCTTCCCA 1920 TCTGTGTTTG 1930
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