| Tag | Content |
|---|
EnhancerAtlas ID | HS042-02526 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:112506060-112507270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:112507072-112507092 | GCTGGTGGGGTGGGGTGGGG | - | 6.91 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AATCTCTCTG TTCCTCAGTT TTCTCACCTG TAAAGTGGGG ATGATAGTAA TGCCTACTTG 60
ATAAGGGTTG CTGTGAAATG GAATTAAACA CAGAGCACTG AGAACATGAC CTGGTCCACC 120
GTATGAGGAT TTTCCTGTCA TTATTACCCT AACAGACAGT CCTGCCAAGG TCCCAATTGT 180
CAAAGAGTTT TTACATGGAG GAAGGGGGCT GACTAGCAGA TCTCTAGTTC CAGTGAGGGC 240
TGATGTGAGG AAGTGAACTG AGCCTACCGT CATGAGGGAC AAAGTCAGAC CTCAGGAGAG 300
ACTTCCTGAC AGCAAGCATT GCTAGACACA AAGAAGGTAA TAGTGGACCT TATGGCTACA 360
TGGCCTTCTG GGGACAGAAA CGCCTAGGCA GGCTGCACTG CCTCTCCATC ACCACACCAG 420
CATGCACACA AGGACTTCTT TTTTGAAGGG CTTCCTGCCT AAGCAAAACC TCAGCTTCTC 480
TCAGAATCAT CTTACGGCCT TCCTTGAGGC ACCATCTCAG GATTCAGAGG GAATTAGTCC 540
TCCCCAAGAA AGAAGAAGAG AAGTCATCCT TTATCCCAAT CCTTAATCCT ACCTACTAGT 600
CAGGGTCTCT GAATTGCTTT CTGATTGTAA CTCTATTGTG ATTCGGCAGA AGGAGGGAAA 660
CAGGCACTTA CATGCCATTA TGGCTGCCCA GGCTCCCAGC CAGGGCCAGG CAGGGAGGGG 720
AAAGGGGCCA ACAGTCTTCC TGGGCCACAA TACTGGGCTC TGGGACTTGA CTGTCTGCCC 780
TGGCTTGACA CACTGCTCTG GTCAAAGCAG ATTTTTCACT GAGGATGGCC CAGCTGGGAC 840
GCTGAGAGCA GTAGGTGGGG AGGGGTGACT CCTGGGCAGG CTGAAGCCCG GGATGCTAAA 900
GTACAGCCTC CCAACCTGCG GGCTGCAGTA CACAGGTGGG TGAGAAGGAG TTACAGGCAT 960
GCAGACTGAT AGAGATTCCC TCCCTCCCCC GGCCCCCACA GCTCCTGAGG CAGCTGGTGG 1020
GGTGGGGTGG GGGCAGCAGA GCCCTGGTCA GTAACCTCCT GCCTCAAGCA GCCTAGCCAG 1080
CCCCAGAGGA ACAAGGTCAA AAGCACAGCC AGGTGACCAC AATGGGAAGC ACAGCTCTAA 1140
GGGAAAACAC CAGCACACTT GGAGCAGGAA AGGCAGCACT AACTCAGAGG GGCTCCTCTT 1200
GCAGCAGAAT 1210
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