Tag | Content |
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EnhancerAtlas ID | HS187-19480 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:55198540-55199960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F4 | MA0470.2 | chr5:55199331-55199345 | TTTTGGCGCCCCTT | + | 6.4 | RELA | MA0107.1 | chr5:55199320-55199330 | GGAAATTCCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I055902 | chr5 | 55198601 | 55200466 |
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Enhancer Sequence | AACTAGAGAA TAATAAGATA ATTTTTGTAA GTATAACTAT CATTAAGTAA TAGTTATCAT 60 ACATTGTCTA CTAGTATGTG TCAGGAATTG TGCTAAGATA ACATAGGTTT TCCCATTTTA 120 GCCTTGACAT GACTCATGAT GTAGATGCTG TGAGATCTAT TTTATAGACG GCAAAGGGAT 180 TCAGGCAAGC TTAGTAATGT GCCCAAGGTC TCTGGAGTGG GATGATTCCA GCTCGGATCT 240 GCAGGATTCC CAACTTGTAC CATATCCCAC AACCTTAGAT GTGTTATTCA TAAAGTGACT 300 TGAATTCCGG TCACAGATGC TGTGTGACAC TGAACTGGTT ATTGACCTGT GCGGGCCTCC 360 ACGTTCCCCT CTTGGAATAA GGGCTTGGAA TGAGGTTCCT TCTGCTCAGC ACGCCCTGGG 420 TTTTGTGAGA CCCGAGACAG CAGGCAGCGG TGGCGTGGTC CCAGGCAGGG CATCGGAAAG 480 CCCGGCCACT GTGTCATAAG GCCAGAGGAG GAAGATGGGC CCAAGTTGGG GCAGAGCTCA 540 GGATGGGCCA GGACGGTTGG CAAAGGAGAA GCAGCACCAG CACGTGAGCC CCGGGTGACT 600 GTCTTCATGC AGATCACAAG AAATCAATGG CTTTCACAGT CAAAGCCCCT CCCTGCTTCT 660 TCAAGGAAGG ATCTGTGTTT CCCACCACAC CTGGGGATGT TTGGAGTAAT TGCTCAGAAA 720 GCTCTTGTTG AATGATGGAA GGACCCGGCG ATTCGTTTAT ATTGAGTAGA GTGATGACTT 780 GGAAATTCCC CTTTTGGCGC CCCTTGGTGT GGCCAGGCTT TCCCCTTTCA AGGTTGACTC 840 ATGGTTTCCT GGGGCCGGCG CCACGCCCCT GTGGTCTCCG CAGTCTCTGC AGTGCACTTG 900 GCGCTTTAGA CCCGGATCTC CCTGCTCCTC AGAGCTCCAG TGTTGGTGAG AAGGAGTGTG 960 GGTTTAGACA CCAACACTGG CTTCTTCAGG CCAGGATTTG TGGGCAATCA TTTTTTAAAA 1020 AAGTGCCTCC AGGGAGATGA GGAAGCTGCA GAAGCAGGCC AGGACAGGGC AGAGGCTGAG 1080 ATGAAGGTGG GCTTTCAGGG CTGCCAAAAC GAAGCACTGC AGACTGGGGG GCTTCAAACA 1140 ACAGAACTTT ATTGTCTCAT GGTCCTGGAG GCCAGAAGTC CCACATCAAG GTGCTGGTTG 1200 GCCATGCTCC CTAAAGTCTC TAGGGGAGAA TCCTTCCTTA CCCCTTCCAG CTTGTAGTGG 1260 CCCCAGGTAT TCCTTGGCTT GTGGTAGCTC CAGTAACTCC CATAAATCCA ATCTCTGCTT 1320 CAGTCTTCAC ATGGCTAGCT TCTTGTGTGT CTCTGTTTCC ATGCCCAGAT TCCTCTTTTC 1380 TTATAAAGGG CCCACTGTCT TAACTAATTA CATCTGCAAT 1420
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