| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33213 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr22:41078820-41079780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr22:41078844-41078864 | GGGGTGGGTGTGGGCTGGGG | - | 6.35 |
| | | 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 |
| GH22I040682 | chr22 | 41078453 | 41082021 |
| Enhancer Sequence | ACTCTGGATG TTCTTGTGGA CTTGGGGGTG GGTGTGGGCT GGGGCGGGGA AGGTGGGCAG 60
CAGAAAAGAG AAAGAGGGGT CACTTGGTTG TGGAATTTAG ATCTTGGTTC ATGCTGCATT 120
TTTAGGAAGC ATGAAGCAGG GATCTGTTTT TCTGAACCCA CAGGGAGGAT TCAGTGGCAT 180
AAATGGAATT ACTGGGGATT CATTAGATTT TGCAGTTCTG CTGCTGGGCT TGTTCTTGGG 240
ACTCAGCTTC CTGTCTTCTG CACAAAATCC CCTGGGCTTT GTTGTCATCA GTGATGAGTC 300
CTCAGGCCCC AAGTCCCAAC CCCCACTCCC CCGCCTCAAC CCTCACCCCC GCTGAGTCAC 360
CAGCCGCAGA GCCAGCTCTT AGGGCAGCTG AAGCCTCTCT GCTTTCTACA GCTGAGATCT 420
GGTGTGGGCA CCTTGAACAG AAGATTACAG CCGGGGCCAC TGGGAGGCAG CCACGACTGC 480
TGCTTGGCTG CTGCTTCTTG GTGTCTTCAC TGAGAGGGGA CTGGGAGCCG TCAGTGCAGT 540
GCTCAGCAGA CCTTACTGAG AGAGCGGGAG AAAGCTGCAA GCATCCTGAA AGCAGGGGCA 600
GCAGCACAGC CTGTTCCTCT TCAGAGCTGC AGCAGGGAGC CTCTTCAGAA AACTTCTGGG 660
CAGCTTCCTT GGGTCCTGGG GACTTTTTTT TTGAGACAGA GTATCGCTCT GTCGCCCAGG 720
CTGAAGTGCA GTGGTGTGAT CTCTGCTCAC TGCAAGCTCC GCCTCCCGGG TTCACACCAT 780
TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG ACTGCAGGCA TCCGCCACCA CGCCCGGCTA 840
ATTTTTGTAT TTTTAGTAAA GACGGGGTTT CACCATGTTA GCCAGGATGG TCTCGATCTC 900
CTAACCTCAT GATCTGCCTG CCTCGGCCTC CCAAGGTGCT GAGACTGCAG GCGTAAGCCA 960
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