| Tag | Content |
|---|
EnhancerAtlas ID | HS049-05721 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr3:128326350-128327860 | 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 | GGGCGTAATG GCGCACGCCT GTAGTCCCAG CTACTCAGAA GGCCGAGGCA GGAGGATGGC 60
TTGAGCCCAG GAGTTTGAGG CCACTCTGAC CAACATAGCC AAACCACATT TCTAAATAAG 120
TAAATGGAAG CGTGGAAGTT GTGCCCTACT GAGAGTGTGT ATGAGAAGCA CCTGAGAACC 180
ACAGCTAATG AACTGCCCAC AGGCTGTGAG GAGTTTGCAC CGGTCCTCAT TGCCTTGCTC 240
AGGGTCAGCC CAGGAGAGGG GCCGCCCCAC CCAACGCTGC CACACAGGCT GGGAAAAGCC 300
ATGGCTCTCC AACGGGCATC CACACTCCCG GCTAAGCAAA GGCTCTGCAA AGCTGGGGCC 360
AGACAGCCAC TCAGTGTCTG CTGTTTCCTC TGGCCCTGAA TCGCAGGCCG CGCTGGATGG 420
CTCTGGTGCC AAAGGGTGGC CTCTGAACAG GAACCTCGGC CTGGGAATGT CCCTGGGACC 480
CCACAGGACC TGACCCGGAG CCACCACTAG AAGCCGGAGC TCCCAGGCCA GGGCTGCGGG 540
AATGGCCCCG GGTCCTCTGC CCAGGGCCTG CAGGTGCTCC AGGTCAGCGG GCGACTTTGG 600
CCGCTGCAGA GACCGAGATA CGCGGGGTAA CAGCCCGTTC CGGAGCCGGT CATCAGGCGC 660
CAAGCCCCGC TGGGCTCCTC GCAGCCGCGG GACCTTTCTC CGCCCTTCCC GAGGCTGAGT 720
TTCCTGAACG GGAAGCTGCC GGCCCGCGGG GCAGCCGGGA GCAGCCAGGG CGTGAGGACG 780
TGGGTTCCCG TCACCCCCGG CTTGGAACAG CAGCGCCGCA ACAACCGCTG GCGTTCATCG 840
AGCCTCTCAG CAGCCCTGCG AGGCGATCCC GGGGAGAATC CCACGCCACA GCCGAGGAAA 900
CTGAGGCAGG CAGGGTGACA CACAGCCCAG TAGTGGCGGG CGGGCGCCCA GGCTGCCACC 960
GCGCTGAGGA CCGGCCCCTC TGCCAGCCGG GAGGTGCGCG TGGCCTAGGC GGGGGCGCCC 1020
TCTGGCGGCC GCGGGTTCCA ATCCCTGCCG GCCTCGCAGG CGTGGGGCAG GACAGCCGCG 1080
CTCTCGCCAG GGCCCAGAGC CCCACTTTGC CAAGGAGCTG TCGCTGGAGC GGTGACTTTG 1140
TTCAGGGCCG AGAACCGGAG GAGGAGGCCA GACTTGCTGC TGGGCAGCTG GCACATGGGA 1200
CATGGGGTGT TATGACTCCA GCATTTATGG AGCGCCTGCT GTGTGCTCTG CAGGTATAGT 1260
CCCATGACCA CCCCCCGAGC ATGGGGTTAT CTCATTCTTT TTTTTGGGGG CGGGGGGGAC 1320
GGAGTCTCTC TCTGTCGCCC AGGCTGGAGT GCAGCAGCGC GATCTCGGCT CACTGCAACC 1380
TCCGCCTCCC AGGTTCAAGC GACTCTCCTG CCTCAGCCTC CTGAGTAGCT GGGATTACAG 1440
GTAGGCACCA CCACGCTAAT TTTTGTATTT TTAGTAGAGG TTTCACCATG TTGGTCAGGC 1500
TGGTCTCGAA 1510
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