Tag | Content |
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EnhancerAtlas ID | HS019-13364 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr5:179731940-179733350 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr5:179732973-179732994 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | Myog | MA0500.1 | chr5:179732589-179732600 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr5:179732589-179732600 | GACAGCTGCAG | + | 6.14 | ZNF263 | MA0528.1 | chr5:179733312-179733333 | GGAGGAGATGGGAGAGGATGG | + | 6.13 | ZNF263 | MA0528.1 | chr5:179733309-179733330 | TGGGGAGGAGATGGGAGAGGA | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 179732228 | 179732341 | chr5 | 179732402 | 179732770 |
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Enhancer Sequence | TGGAAACAGG AGGTGAGATC AGAGTCACAC TGGGCAGATG GGGCTGGAGC AGATCAGCCA 60 GAGGGGAAGA AGGGGAACCA GGGGAAGGAT GACTCTGGAA GGCAGAGAGC CAAGGGTTGC 120 AAGGCAGACA GATGCCTGGA GTGCTTGACA GCACTGAGGA CACCCAGCAA GGGCCTGGGG 180 AGAGGCCTGG CTACCATCCA GAGCATGCAC CAGCCCGGGA CACAACCTCT GTGTCCCCAC 240 ACCAGCCCCG GGCACTGCTG TTGTCTCTCT CCAGTCCCAC GCACAGCCAC CCCTTAGGAC 300 AAACAAGTCG GAGTCAGCCT AGCTCACCCC CTGCTCCTCC CTAGCCAGCC ACGTGTATAA 360 CGACAGCATC GTATTCAGCT TAGCTACACC TTCAGTTAAT TATCTGATTA AGCATTTGCC 420 CATTAATAAC TTCTAAAGAG TGGTTCCAAG CAAAATCACA CAAACTGGGG TGTTATTTGA 480 ATTAATTTTT TTCCTGTGTT CAGGTAGATC CATCTCTATT CAGTTACCAC AAATCCACGT 540 CATTGAAATG GTGAGACAGT CAAATAAATC ATCTCTCGAC TCCCCGCTAG CACTGCTGAT 600 TTAGGTCAGG GCCACACTGT AAGGAGTGCG GCTCCAGTCT GGAGGCGCAG ACAGCTGCAG 660 TGCCGGCCTC CCAGTGACCA GAGGACCATG GGCTCGTGCC AGCAGCCACC TAAACGCTTC 720 TTCCTTCAGC AGACTCATGC GGAGGCATAG CTGCAATGTG CATCTCCCGC CAGCACGTTC 780 AGCCACCGCA GCTCAGCCCC CACCCATGAC GCAGAGTCAT CTGGGGACTG ACAGTGCACC 840 CCAGGCCTTG CCTCTACTGC ACTCCAAGAA GCAGCACCTG CCTGTTCTTT AACAGGAGTC 900 AGAATCTCCA GGGGGCAGGT GCAGGAGATG GAGCTCAGTG AGGACAGCCC TGCACTCCCC 960 ACCAAGACCA AGGAAATCAA CTCTGAATGT TTCCGGTAAC CACTTGTAAC TGGCATTGTC 1020 TTTCTTTTTT TTTTCTTTCT TTCTTTTTTT TTTTTTTCGT TGAGATGGGA GTCTCGTTCT 1080 GTCTCCCAGG CTGGAGTGCA GTGGCATGAT CTTGGCTCAC TGCAACCTCC TCCTCTTGGA 1140 TTCAAGCGAT TCTCCTGCCT CAGCCTCCCA TGTAGCTGGG ATTACAGGCG TGCACCACCA 1200 CGCCCAGCTA GTTTTTGAAT TTTTGGTAGA GATGGGCTTT TACCATGTTG TCCAGGCTGG 1260 TCTCGAACTC CTGACCTCAA ATGATCTGAC TGCCTTGGCC TCCCAAAGTG CTGGGATTAC 1320 AGGCGTGGAC CACTGTGCCA GCCTAGCATT GTCTTTCAAA TGGGGGTGGT GGGGAGGAGA 1380 TGGGAGAGGA TGGCAGCCCA GCTGGGCCAC 1410
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