| Tag | Content |
|---|
EnhancerAtlas ID | HS127-12498 | Organism | Homo sapiens | Tissue/cell | Macrophage | Coordinate | chr16:88665120-88666190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr16:88665783-88665797 | CACTTCCTCATTTT | - | 6.59 |
| | | 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 |
| GH16I088598 | chr16 | 88664728 | 88666846 |
| Enhancer Sequence | GTAAACACAA TTCAGCAGAA ATCCCGACAA GAAAGATGCT ATTACAGGAG TGGTTCTTGA 60
CAAAACTGGG ATTTCCTCGG TCCAGAGAGA GCCCCAGAAA TCTCTGAAGT TAGGCGTCTG 120
TTTCTGTGGT GTCTTTCTTT ATTTTTTATT TATTTATTTT TTTGGAGACA GAGTTTCACT 180
CTTGTTGCCC AGGCTGGAGT GCAATGGCCC AAACTCGACT CACTGCAGCC TCCGCCTCCC 240
AGGTTCATGT GATTCTCCTG CTCGGCCTCC CAAGTAGCTG GGATTACAGG CATGCGCCAC 300
CAGGCCCGGA AGGATGGAGA GTTATATCTA ACTGTCTCAG GCAGCAGCCC AGTAGGCCAG 360
GGAGTTCAGT CCAGGGCATA CCCACTGTCT TCATGGGGCT GGATCAGCAC TGGGCCACAC 420
CCCAGCTGGC ACTGCCCAGG AGCACAGGGT GCAGTCTCCA GCCACTCACA GAAAGCCTGG 480
CGAGGCTGCC CGAGCCGCAC CCCCAGGATC TGCACCCCAC ACTCCTGAGA CTCAGTGTCT 540
GCTCTTCCTG GAGAAAACTT GGAGCTTTCT GGTCCTATCA CTGCACACTT CCTCCCTCTA 600
GGCCCACGTT GGCCCCAGTG TGTGAGCTTC AGCTCTGGGG ACCACTCTGC TGGCACCCAG 660
CCCCACTTCC TCATTTTCCT GGTCAGCCTC CCTGCTGGGA AATGACGGAC AAGATGTTCC 720
TTCTCACTCC CTCGGCATGT CACTTCCTTC CCTCTGAGAC TCCAGCCACT CCACCTGCTG 780
CTTGTCACTG AGTGACTGAA CCCTGGATCT AGTTCCAAGG GTAGTTGAAG GAAGTGATGA 840
ACACCTCATG TGGGCACACG GAGGCCGGGG GCAGCTGTTT GTGCAGAGAC GGGCACAGAC 900
TGCCCTCCCC AGAAGGACAA CTGTGCTGTG TCCGCCCCTC ACCCCTTGAG CACTTGCAGC 960
GTGCAGCTCC TGCTCCTGCA GGGCTGCTGC GGTCGGGTGG GACGGCTCCC TTTGTGTTTC 1020
CTAACAGCGA CGCCCGGTAT TCTGTTCCAT GTTGACTTCT TTCTTCTTAC 1070
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