| Tag | Content |
|---|
EnhancerAtlas ID | HS098-42124 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr4:54568240-54569660 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIL3 | MA0025.1 | chr4:54569032-54569043 | ATGTTACATAA | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 54568898 | 54569145 | | chr4 | 54568519 | 54569562 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH04I053701 | chr4 | 54567859 | 54570101 |
| Enhancer Sequence | AGAAAGAGAC ACAAAGGAGC TTTTCACATA AGGGCGATGG ATATATTCTG TATCTTGATC 60
AGGGTAGTAG TTACGTGGGT GGATACATAG GTGAACAAGT TTATCAAACT GTCAGTTTCA 120
GATTTCTACA TTCTTGTGCA TATAAATTTT CCTAAACTTG AAAAAGGCCG TCTTATCCCC 180
ATCTTTCCCA ATGGAATCTG TGTTTCAAAA AGATAACAAT ATAGTGTTCA TGCCTTCAAA 240
CAGGCCTGGT AGAAAGGAAA TTAACATACA TTATTTATCT CGTATATATG TATGTTTCTG 300
CCTGTAATAA ATAATGGGGA TTGAGCACTT AGCACAAGAG TAAGCAACTG CCAAATGCAG 360
CTCTGGGTTC AGACCTGTAT GGGGCAGACC TGAGAGCCAG GCCCCTTTCC CTACCATACT 420
GAAACTGACA GCAAAGCCGC TCAGCTAAGG GGATGTGCAG AAAGGACGCC CTGGGGTCTC 480
CTGAGGCTGC AGGGCGGCCG GGGAGCCCTG GGGTCAGGAG GGCAACTTTC TGGGGCACAG 540
TGCTCGAGTC ACCTCTCCGA GGAACGGCTC TGCCTGCACT GCTTCTTGTA CTTTGTTTAC 600
CCGCCCCTAG GAAAAGAGCT GTGAAGATGA TCGTAGGGAG CAAGCAGTGA GGCGGCAAAT 660
GGCTCTGAGA GGAGCCACGC AGACAGCTGG GCAGCCGTGC CAAGAACAAC AGGAAGCTCG 720
CGGCCCCACC CCTGCTCGCT GCAGCCCTGG CCTGGAGACC CAGGGTTATT TGCTTTGAAG 780
GGCCCTCTGC AGATGTTACA TAAACAAAAC CTCCATTGAC TCCAGTTCTG AGCCTGGCCT 840
AAAATAGCCC GCGGGCTTCC CCCTACCACT GTGCAGTTTC GCCGCCATCC CTTTTGGTCC 900
CCTTGTGTGC TAGCTGCTTC CCTCCATTGA CCACATGTGC AGACAACTCT CGCCAGTGTC 960
CCTAAGAGGC CAGTTCCCTG GGGAACAAAA AGTGGGGCTC GTTTGCCTTC CCTGGCAGGT 1020
CAGACACAAA GCATCCCTGT AAGACCTTTG ATGGCTACTG GCCAAGGGAC ACGTTTCCCC 1080
TCCCCAGGGA GGCAGGAAGC TGGGCTGAGG CACAGTGGGG TTTGGTCAGC AGCCAGCACA 1140
AGAGGGACTG TGCTTTCTCT CTGTGTCTGT GTCTCTTTCT GTGTGTGTCT GCGTCTCTCT 1200
CTCTCTCTGT CTCTTTCTCT CTCTTTCCTA AGGGCAAGCT CTCCAGGTAA GGGCACGAGT 1260
TCTTCGTCAG CGTCTCTATT TTCACTTGAT GTAACGACTG AACACTCTAC TCTTGACTCT 1320
TCCTCCAAGC TCCTATAAAA TTCCCTGACC CCATTTGCAC TTCAGCTCCT TCATTCTGCA 1380
GAAAACCATT CCTTCGTGAA CATCTGGAGA ATCACAGATC 1420
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