Tag | Content |
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EnhancerAtlas ID | HS182-11492 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr19:45675460-45676350 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr19:45676252-45676263 | CCACACCCTCC | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 45676215 | 45676348 | chr19 | 45675809 | 45675980 |
| | Number: 1 | ID | Chromosome | Start | End |
GH19I045170 | chr19 | 45673860 | 45678046 |
| Enhancer Sequence | GGACAGAGAT GAAGGAGCCA CCATCCCTGT CCTCAAGGAG CTCTGAAGCT GGTGGGAAAG 60 GCGGCCTGTG CTACCCAGAA GCCCTGGGGC CAGAAGCCTG AGTTCTAATT TTGCCTTTAA 120 GAGAACATTC TGCCCTGAAC TGGGAGGGAG GCGGGTGGGG GCCATGTGCT CCACCCCTTC 180 CTGTCTCTTG TGTCTGCCCT ACCCCTCGAT TGTTCTCTAG GCACCTGCTA GCTCCTGGGC 240 AGAGGCTGAC CCTGTTCAAC GCCCACCTGC TGAGCCACTC TGTGCCAGGC CCAGGGGTGT 300 GGTGGGGAAC CCAGGGAAGG AGCAGCCCTG GTTAAGAAAA GCACACAGAC AGAAGTGCTG 360 GCACACAGAT GGGTGAGTGA GGGGTGGGTG CGAGAAGCCT GCAGGACTTC CCTGCTGTTG 420 CCCTCAACTC TCCTCCCTGG TCCAGCAAGG CATCCTGAGC AAGTCCAGAT CCTGCCTCTG 480 CCCACTCAGA ACTCCCCATC CTGTCCCCTG GCCCAGCCCG GAAGGTTGAG CCCACCACAG 540 CCTCTGCCTT AAGCTCCTGC AACAGCGGGG CCCTTCCCAG GCCAATCTCC ATCCAGTCCA 600 TTCCTGTGGC CAGGGAGACA TTTCTAGAAT GTAAATCTGA GCCAGGCGCA CCTCAGTTTA 660 AACCCGGCTA TGGCTCCCAC TGCCTTCGGG ATGGAGCCCC AGTTCCCAGG AGGGCCTCGC 720 TGGAGCTCCC AGCCACAGAT GCTCAGGACG GTGTTCCGGG CAGGGACCTA TCTGACAGCC 780 GCTCCGCCCG CCCCACACCC TCCTCAGATA AGGGGCTGCC CAAGTGCACT CTCGGGGTGT 840 GGTGGATGGA GGCCTGGCGC AGCAGGGCTA TTCTCGGGGC GCCTCGGGCC 890
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