| Tag | Content |
|---|
EnhancerAtlas ID | HS047-16314 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr19:1029460-1030510 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:1029697-1029718 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 1029998 | 1030409 | | chr19 | 1029563 | 1029774 |
| Enhancer Sequence | CCCAAATCAT CCTAGGCAGG TCCAGCTCAG GGGACCCTAA CCCAAATCAT CCCAGGCAGG 60
TCCAGCTCAG GGGACCCTAA CCCAAATCAT CCCAGGCAGG TCCAGGTCAG GGGACCCTAA 120
CCCAAATAAT CCCAGGAAGA GATGAGGAAG CGGAGGCTGA GTGGGGAGCT GTCCGCGGGA 180
ACCTGGGGAG ATGGGTGCAG AGCAGGGAGA GGGATTTGAT TTTTTTTTTC CTTCTCTCTT 240
TTCTTTCTTT TTTTTTTTAA GACAGAGGCT CACTCTGTTC CAGGCTGGAG TGAAGTGGCC 300
CGATCTTGGC TCACTGCCTC CTCTGCCTCC TGGGTTCAAG CGATTCTCCT GCCTCAGCCT 360
CCCAAGTAGC TGGGACTACA GGTGCCCACC ACCACGCCCA GCTCATTTTT GTATTTTAGT 420
ACAGACGGGA TTTCACCATG TGGGCTAGGC CAGTCTCGAA CTCCTGACCT CAGATGATCC 480
GCCCGCCTTG GCCTCCCAAA GTGCTGGGAT TGTAGGTGTG AGCCACCGCA CCCAGCCCAA 540
ACCCTACTTT ATTCTCCCTC CAGCGTTTAT CTCCCGCTCC CGCTACACGA CCTGCCCCCA 600
TGCTTATGGC CCCCTATACA CTTTGCCGTC TGCCTCAGTG CTGTCTCCGC GGTCACTAGT 660
GGCTGGATAG GGACACTCGA GGTCCCCACT GGTGCACACC CACTGCCCAG GAGCACACAG 720
CCCATTCCCC ACGGCGGTGT CTCAGAGCAC CGAAGGCCAA GAAAGCTGGA ATGGCCGGGT 780
GCAGAAAGGT GGCAGGGAAT CGGTGGCAAG GAGCCAGGTG CGTGACTAGA GGCGGTCAGC 840
CTCGGGGGCA GCTCCTTCGG GAGTTGCTAA GAAGCAGGAT GGGGGCCGGG CGCGGTGGCT 900
CACACCTGTA ATCCCAGCAC TTTGGAGGGC TGAGACGGGC AGATCACGAG GTCAGGAGAT 960
GGAGACCATC TTGGCTAACA CGGTGAAACC CCGTCTCTAT TAAAAATACA AAAAATGAGC 1020
TGGGCCTGGT GGCGGGCGCC TGCAGTCCCA 1050
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