Tag | Content |
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EnhancerAtlas ID | HS182-00531 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:27264280-27265610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr1:27264738-27264750 | TGCTGTGATTGG | - | 6.02 |
| | 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 |
GH01I026937 | chr1 | 27264268 | 27265453 |
| Enhancer Sequence | CTACAGGTAC CACTACACTC AGCTAATTTT TGTATTTTTT ATAGAGACAG GGTCTTCCTA 60 TGTTGCCCAG GCTGGTTTCA AACTCCTGGG CTCAAGTGAT CTGTCTGCCT CTGCTTCCCA 120 AAGTGCTGGG ATTACAGATG GGAGCCCCCG TGCCCGACCT GGATTAGCAT TTGAATAACA 180 GCTATTTCAT AAAATTCTTC TGCCTTCTGA AAAGTATTTG AGAAGGCTGG CATGGTGGCA 240 CATGCCTGTA CTGTCCTGGG CCTCTTCTGG GGGAGAGTGA CAGGCTTGGA TTTAGAGCAG 300 GCCCAGCCCT CCCCACCCTG GTTGGCTGTG GTTCCCAAAG ATGTGTCCAG TGACCGAAGC 360 TTGAGTCGGT GACAGCCTCT GGGTAAGCTT CCACAACCCT GGGGTTATCT GTCTGAGGCT 420 GGGCCTAGGT CAGGCTGATG GGAGGATGGG TCAGAGGCTG CTGTGATTGG CCTTGACTCT 480 GCCTGGTGGT TTAGCTCTGC CCTTGCTTAA CCTCCAGGAG CTAGGAAGGA AGTACAAATG 540 GGATGTGACA TGATTCAGTG GAGCTGGGAG AGGGGAGGGC CCTGCTCCCA CCTCCCTTTG 600 GCCACTGGTT GGCAAATGCC TTTAGTTCAA GGTCTCTCTG ATTAGGGACT TAGGACCAAG 660 GCCTTGTGGT GGAACAGCCT CTGCTGGTGT AATTATGACC TATTGTTTCT ACTGACAGCA 720 GAATGGCCTC CCCTACCAGT TTAATTTGTG GTTTAGGGGG TACGTTTGGT GTTCTTTAAC 780 CTTGTAGAGT GTGGAGCTAC TGTGGTGTGG CATGGGACAG GGGGTTTGGG CATAGCAGGA 840 GAATTTGGCG TCAAATGGGT GAGAATCCAC AGGGCATTTA GCAGAACCCC AGGTCTGGGG 900 GCCCGTGGGT GACTTCTGTG ACCTTGAGCC CCTGCAGAGC TTTCCCTGCA GTTCTGCCTT 960 AGAGATGCTT GAAAGAGGGT TTATTGACCA CTGATCACAT GGCAAGTGCC CTGCAAGGCC 1020 TCTAGGGGTA TGTGCGTATG TGTGCACATG CACACTGTGT ATGGGTTGGC ATTGAGTTGA 1080 GTGTCCTAAG GGTATGTTCC TGGCCAGAGG TGAAACTTTG ACACTTGACT GGTCATGGAG 1140 GATGAATTGG TTTGCCAGGT GACCTGAGAA TGGGGATGAG ACATTCTAGG CAAAGAACAA 1200 CACATGCCAA GATTGCTTTT ATTTATTTTG AGACAGGGTC TCCCTCTGTT ACCCAGGCTG 1260 GTGGCGCGAT CTCTGCTCAC TGCAACCTCT GCCTCCCGGG TTCAAGTGAT TCCCCCACCT 1320 CAGCCTCCCA 1330
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