| Tag | Content |
|---|
EnhancerAtlas ID | HS062-11625 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr3:128326810-128327870 | 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: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I128607 | chr3 | 128326539 | 128327930 |
| Enhancer Sequence | CTGGGAATGT CCCTGGGACC CCACAGGACC TGACCCGGAG CCACCACTAG AAGCCGGAGC 60
TCCCAGGCCA GGGCTGCGGG AATGGCCCCG GGTCCTCTGC CCAGGGCCTG CAGGTGCTCC 120
AGGTCAGCGG GCGACTTTGG CCGCTGCAGA GACCGAGATA CGCGGGGTAA CAGCCCGTTC 180
CGGAGCCGGT CATCAGGCGC CAAGCCCCGC TGGGCTCCTC GCAGCCGCGG GACCTTTCTC 240
CGCCCTTCCC GAGGCTGAGT TTCCTGAACG GGAAGCTGCC GGCCCGCGGG GCAGCCGGGA 300
GCAGCCAGGG CGTGAGGACG TGGGTTCCCG TCACCCCCGG CTTGGAACAG CAGCGCCGCA 360
ACAACCGCTG GCGTTCATCG AGCCTCTCAG CAGCCCTGCG AGGCGATCCC GGGGAGAATC 420
CCACGCCACA GCCGAGGAAA CTGAGGCAGG CAGGGTGACA CACAGCCCAG TAGTGGCGGG 480
CGGGCGCCCA GGCTGCCACC GCGCTGAGGA CCGGCCCCTC TGCCAGCCGG GAGGTGCGCG 540
TGGCCTAGGC GGGGGCGCCC TCTGGCGGCC GCGGGTTCCA ATCCCTGCCG GCCTCGCAGG 600
CGTGGGGCAG GACAGCCGCG CTCTCGCCAG GGCCCAGAGC CCCACTTTGC CAAGGAGCTG 660
TCGCTGGAGC GGTGACTTTG TTCAGGGCCG AGAACCGGAG GAGGAGGCCA GACTTGCTGC 720
TGGGCAGCTG GCACATGGGA CATGGGGTGT TATGACTCCA GCATTTATGG AGCGCCTGCT 780
GTGTGCTCTG CAGGTATAGT CCCATGACCA CCCCCCGAGC ATGGGGTTAT CTCATTCTTT 840
TTTTTGGGGG CGGGGGGGAC GGAGTCTCTC TCTGTCGCCC AGGCTGGAGT GCAGCAGCGC 900
GATCTCGGCT CACTGCAACC TCCGCCTCCC AGGTTCAAGC GACTCTCCTG CCTCAGCCTC 960
CTGAGTAGCT GGGATTACAG GTAGGCACCA CCACGCTAAT TTTTGTATTT TTAGTAGAGG 1020
TTTCACCATG TTGGTCAGGC TGGTCTCGAA CTCCTAACCT 1060
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