| Tag | Content |
|---|
EnhancerAtlas ID | HS047-17902 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr19:49410540-49411990 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr19:49411118-49411130 | CGTCAGCATTTT | - | 6.74 |
| | | 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 |
| GH19I048906 | chr19 | 49409738 | 49412844 |
| Enhancer Sequence | TTTTTTTGGT GAGACAGAAT CTTGCTCTGT CTCCCAGGCT GCACTACAGT GGCGCGATCT 60
CGGCTCACTG CAACCTCCGC CTCCTGGGTT CAAGCAATTC TCCTGCCTCA GCCTCCCAAG 120
TAGCTGGGAT TACAGGTGTG TGCCACCACA CCTGGCTAAT TTTGTATTTT TAGTAGATAC 180
TTGATTTTGC CATGTTGGCC AGGCTGGTCT TGAACTCCTG ACTTCAAGTG ATCCTCCTGT 240
CTCGGCCTTC CAAAGTGCTG GGATTACAGG CCTGAGCCAC CAGCCTTGGC CCCCATCTTA 300
AGGTCTTTAA TGTAATCCCA TCCGCCAGGA CCCCTTAGCC CGGAAAGGTC ACGCATTCAC 360
AGGTTCCGGG GATCAGGATG TGGATATCTT TTAGGGCACC AGTATCCAGC TGCCACAACA 420
CCCAGGCTCT TCCCGTCCCT CCTCTGCCCA GAGCCTGCCC CCGGCACCCC AGTGCCCTCA 480
GGCCCGCATT CATGTTCCTC TTGTCTGCTC GGAGCCTGGG TGGACCTTGG CCACACCCGC 540
CCAACCCTGC CCTTCCCGTA TGCACCCTGA CCTTCTTGCG TCAGCATTTT TAGAAATTGC 600
TGGCGTGCAG CCTTGGGACC TTTGTCCGTT CGCCCCGCTC TCCCGTGACA TTCTTTCTCA 660
GGGCTCTTTG CCTGGTCCAT GGACCTTCCA TCTCCCCTGG AATGTCACCT CCTCAGGGTG 720
TCACCGCCCC GGCTGTCCTG TGTGAAGGAG CCTCTGTGTT ATTTGTGTCC TTGGTATTCC 780
TTTGTTCATC CCTTGGTCGC CTGTTCTCTG TCTCTCTAGA CTGGGTGCTC CAAGAGGCAG 840
AACTCTTTTG GTTGTTGTTG TTTTTGAGAC AGAGTCTCAC TCTGTCGCCC AGGCTGGAGT 900
GCAGTGGCGC GATCTCGGCT CACTGCAACC TCTGCCTCCC AGGTTCAAGC GATTCTCCTG 960
CCTCAGCCTC CTGAGTATCT GGGATTACAG GTGCCCGCCA CCATACCTGG CTAATTTTGT 1020
ATCTTTAGTA GAGACAGGGT TTCACCATGT TGGCCAGGCT GGTCTCAAAC TCCTGACCTC 1080
AGGTGATCCA CCCGCCTCAG CCTCCCAAAT TGCTGAGATT ACAGGCATGA GCCACCCCGC 1140
CTGGCCTCCA AGAGTCAGAA TTCTGTCATC ATTTGATTCC TGCTGTGTCC ATAGCGGCCG 1200
GCGCTGGGTC AGCCTGGAAT AGCGGCTCAA CACACGTCCC TGGCACAAAT AATGAATTTG 1260
AGATTCAGTT TGTACCTGTG TCCTGCACAC CTGTCACTCC TCTGGGCTCA GCCAGGGCCG 1320
GAGCTGCCTC CACTGCAGCC TAGGTCTCCC AAATTCTAGC TGCCCGTGTG TGTGTGTGTG 1380
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTCTTTC TGCCCACTTG ACCAAGGGGT 1440
GTGTGTGTGT 1450
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