| Tag | Content |
|---|
EnhancerAtlas ID | HS182-10642 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr19:1029520-1030510 | 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 | TCCAGCTCAG GGGACCCTAA CCCAAATCAT CCCAGGCAGG TCCAGGTCAG GGGACCCTAA 60
CCCAAATAAT CCCAGGAAGA GATGAGGAAG CGGAGGCTGA GTGGGGAGCT GTCCGCGGGA 120
ACCTGGGGAG ATGGGTGCAG AGCAGGGAGA GGGATTTGAT TTTTTTTTTC CTTCTCTCTT 180
TTCTTTCTTT TTTTTTTTAA GACAGAGGCT CACTCTGTTC CAGGCTGGAG TGAAGTGGCC 240
CGATCTTGGC TCACTGCCTC CTCTGCCTCC TGGGTTCAAG CGATTCTCCT GCCTCAGCCT 300
CCCAAGTAGC TGGGACTACA GGTGCCCACC ACCACGCCCA GCTCATTTTT GTATTTTAGT 360
ACAGACGGGA TTTCACCATG TGGGCTAGGC CAGTCTCGAA CTCCTGACCT CAGATGATCC 420
GCCCGCCTTG GCCTCCCAAA GTGCTGGGAT TGTAGGTGTG AGCCACCGCA CCCAGCCCAA 480
ACCCTACTTT ATTCTCCCTC CAGCGTTTAT CTCCCGCTCC CGCTACACGA CCTGCCCCCA 540
TGCTTATGGC CCCCTATACA CTTTGCCGTC TGCCTCAGTG CTGTCTCCGC GGTCACTAGT 600
GGCTGGATAG GGACACTCGA GGTCCCCACT GGTGCACACC CACTGCCCAG GAGCACACAG 660
CCCATTCCCC ACGGCGGTGT CTCAGAGCAC CGAAGGCCAA GAAAGCTGGA ATGGCCGGGT 720
GCAGAAAGGT GGCAGGGAAT CGGTGGCAAG GAGCCAGGTG CGTGACTAGA GGCGGTCAGC 780
CTCGGGGGCA GCTCCTTCGG GAGTTGCTAA GAAGCAGGAT GGGGGCCGGG CGCGGTGGCT 840
CACACCTGTA ATCCCAGCAC TTTGGAGGGC TGAGACGGGC AGATCACGAG GTCAGGAGAT 900
GGAGACCATC TTGGCTAACA CGGTGAAACC CCGTCTCTAT TAAAAATACA AAAAATGAGC 960
TGGGCCTGGT GGCGGGCGCC TGCAGTCCCA 990
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