Tag | Content |
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EnhancerAtlas ID | HS182-17777 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr5:132465480-132466750 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr5:132466630-132466644 | GTGAGTCATCCCTT | - | 6.29 | ZNF263 | MA0528.1 | chr5:132466263-132466284 | GCTCCCTCCCTCTCCTCCCTT | - | 6.09 | ZNF263 | MA0528.1 | chr5:132466254-132466275 | TCCTCCCTTGCTCCCTCCCTC | - | 6.3 | ZNF263 | MA0528.1 | chr5:132466317-132466338 | CTCTCTTCTCTCTCCTCCCCT | - | 6.61 | ZNF263 | MA0528.1 | chr5:132466314-132466335 | TTCCTCTCTTCTCTCTCCTCC | - | 7.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 132466434 | 132466734 | chr5 | 132465603 | 132465974 |
| Enhancer Sequence | TACTGTATAA TTGAAAGAAA ACTGGACCTC CTTTTATTAA TACAATCTCA GTACAATTAT 60 GCATCTAAAG GAAATGCACA AGGCCCTAGA AGCCTTGTGA GGGTCATGAA CAGAGTTGCT 120 GAAGGTTTCC TTAGGGGGGT TGCCAATGGG GAGTTATTTG GCAAATTTCC TAAATGTTCT 180 CTCTTACCCG TTTATTTCCC TGATGCCTGG ATTTTCTAGC AACTGCTGAG CTCTCTGCTT 240 TCTCTTCAAA ATGCTCAATC TCTGGGCTGG CTTTCTTCTC TCTGGCTCTG GCCAAGACCA 300 TTTAAACAAC TTCCAGCTCC AAACTTTTGT TTTCCTTCCA GCAAAGGCAA GCCCATCCTT 360 CTGCAGATGA TTTAGACTCT GGCTCATTCC TGTTCTCTTC TGGTTTCTCA CCCTGATCAG 420 TATGATGAAG GGAGCCCGCC AAGCAGTTTT GGCCAAACGT GCCTGGGGTA ATTCTAGCTT 480 TTGGATGTGC AGACTGAGCT ATGAGTGGCA GCCTCTGAAA GATGAAGGCT GAGGTGGAGA 540 GAAGTCAGGG ATGCTGAATG AGGTGCCCTC AGAGTGCTCC TGCCATCCTG AGATTTCACC 600 TTTAGAAATG TGTTAGAAAA TTGTCCTTGA GTAACAGAAG CCCACTTATA CTAGTTCATG 660 GCAAAAATTA TTATAAAGAC ATAGGAGTTG ATTTCAGAGC CTGAGACCAG GAAGGAAGCT 720 GGAGCTCGGG AATGGGCGGA GACTAGAACC TGGAAAGTTG TCAATTTCCT CACTTCCTCC 780 CTTGCTCCCT CCCTCTCCTC CCTTCGATTC TTCTCTCTCC CTCCCCCCTT CCACTTCCTC 840 TCTTCTCTCT CCTCCCCTCT TTTTTCTCTG TAGACCAGCT TTCTCTGGCC ATAACGGGGA 900 AGATGGCCAC CCCCACACTC TTTGAGCTTT GCTTGGCTCT CAGTTCCAGT CCCACGAGGA 960 AGTTAATAAC TGAGTCTACC TGGAGAAGAT TCTCACTGAC CCACCTTGGG GCAGGTAATC 1020 TTCCCAGGTA ATAGGTCCTG TCACCTCTGG CCAGGGAGAT GTGCTTCTGA GGTGCACACA 1080 TGGCTGCCGT GACCCACACT TGTGGTGTGG GAAGGCAGTT TTCAGGACAA TGGGATGACC 1140 CATGGGCTGG GTGAGTCATC CCTTTAAGGT GTTTCCCGCA GGAGGCACTT ATGTGACAAA 1200 TCCATCACCC AAGTGGGGGA AATGCTTATG GGGCTCCTGT TGCTATTAAT GTGGCTAATC 1260 AGACGACATA 1270
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