| Tag | Content |
|---|
EnhancerAtlas ID | HS047-24501 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr3:128326520-128327650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:128327362-128327381 | GGGCGCCCTCTGGCGGCCG | - | 6.88 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 128327283 | 128327483 | | chr3 | 128326600 | 128327239 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I128607 | chr3 | 128326539 | 128327930 |
| Enhancer Sequence | CCTGAGAACC ACAGCTAATG AACTGCCCAC AGGCTGTGAG GAGTTTGCAC CGGTCCTCAT 60
TGCCTTGCTC AGGGTCAGCC CAGGAGAGGG GCCGCCCCAC CCAACGCTGC CACACAGGCT 120
GGGAAAAGCC ATGGCTCTCC AACGGGCATC CACACTCCCG GCTAAGCAAA GGCTCTGCAA 180
AGCTGGGGCC AGACAGCCAC TCAGTGTCTG CTGTTTCCTC TGGCCCTGAA TCGCAGGCCG 240
CGCTGGATGG CTCTGGTGCC AAAGGGTGGC CTCTGAACAG GAACCTCGGC CTGGGAATGT 300
CCCTGGGACC CCACAGGACC TGACCCGGAG CCACCACTAG AAGCCGGAGC TCCCAGGCCA 360
GGGCTGCGGG AATGGCCCCG GGTCCTCTGC CCAGGGCCTG CAGGTGCTCC AGGTCAGCGG 420
GCGACTTTGG CCGCTGCAGA GACCGAGATA CGCGGGGTAA CAGCCCGTTC CGGAGCCGGT 480
CATCAGGCGC CAAGCCCCGC TGGGCTCCTC GCAGCCGCGG GACCTTTCTC CGCCCTTCCC 540
GAGGCTGAGT TTCCTGAACG GGAAGCTGCC GGCCCGCGGG GCAGCCGGGA GCAGCCAGGG 600
CGTGAGGACG TGGGTTCCCG TCACCCCCGG CTTGGAACAG CAGCGCCGCA ACAACCGCTG 660
GCGTTCATCG AGCCTCTCAG CAGCCCTGCG AGGCGATCCC GGGGAGAATC CCACGCCACA 720
GCCGAGGAAA CTGAGGCAGG CAGGGTGACA CACAGCCCAG TAGTGGCGGG CGGGCGCCCA 780
GGCTGCCACC GCGCTGAGGA CCGGCCCCTC TGCCAGCCGG GAGGTGCGCG TGGCCTAGGC 840
GGGGGCGCCC TCTGGCGGCC GCGGGTTCCA ATCCCTGCCG GCCTCGCAGG CGTGGGGCAG 900
GACAGCCGCG CTCTCGCCAG GGCCCAGAGC CCCACTTTGC CAAGGAGCTG TCGCTGGAGC 960
GGTGACTTTG TTCAGGGCCG AGAACCGGAG GAGGAGGCCA GACTTGCTGC TGGGCAGCTG 1020
GCACATGGGA CATGGGGTGT TATGACTCCA GCATTTATGG AGCGCCTGCT GTGTGCTCTG 1080
CAGGTATAGT CCCATGACCA CCCCCCGAGC ATGGGGTTAT CTCATTCTTT 1130
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