| Tag | Content |
|---|
EnhancerAtlas ID | HS184-25205 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr5:156873830-156874980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr5:156874741-156874759 | GGAAAGTGAAACCCTAAC | + | 8.56 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I157446 | chr5 | 156873836 | 156874971 |
| Enhancer Sequence | GCACTATTCT CTGTGAAGTT CTGGTTCAAT AAAAAATGCG CATTCAAAAA TATAGGATGT 60
TCTCCCCCCT TTGGCCAAAA ACCAAGGGTT ATTGACCTGT ATCCTTCTGA AATTCAGTGC 120
AAAAGTGATG TGTGCCTCTT TCTGGGCAAG TGTTGACCCT TTTTGTCAGA TTCTTAAAGG 180
GATTTGGAGC TCCTAAAAAG TTAAAAATTA CCAGTGAGGG CCTTCCCTAA AATAAAGACC 240
ACTTACTTCT GGTTTTGTTG GGGTTTGACT AAAGGTCAGA CCGCTCTGTC AGAACAGGCT 300
TTCTGGAAAT GCAGACCTTG AGATAGGTAA GCACCAACGT ATTTAATGGG CTGGCTACAG 360
AATAAACAGC TACATTTTTC TTTGGGGAGC AAAATGCAGA TAATTATCAC CACTTAAGCT 420
TTAGTGCAAC TGTGTAAAAA GGCGCGGCTT TTTATTGGCC CAGCGCCTTT GTGTGCAACC 480
AATCCTGAGG TGGGCGGCTG TGTCCCCGCC CTGGTGGGCG GAGCTCTTCC CAGCCCAGGG 540
GCCTTTGCCC ATCAGGCGGT TCCGCCTGGC ACTGGCTGGG CGGAGGTCCT TGGTAGCAGA 600
GGGGCAAATT AACCCTCTGC CTCACTTGAC AAGCCTGAAG AAAGCTTAAC CCACGCTCTG 660
GATTCCTCTG GGGTCCCTTA TCCAGGCCAG GCCCGCAAAC CAGAATTTCC AGTGTGACCG 720
TGTTGGCAGA GAGTTAATGA GCAGCCAAGG AAGCTGTGGC TGTTGCTGTT GTAGACTTGC 780
CCCAGAGGGA AGGACAGAAG AACGCCAGGT CCTTCCTTAG CCTCTCTGCT TGGAACGAGG 840
CAGGTGGGAA GGGTGCATCT CAGTAAGTGG AGGCTAGACA TGAGATTGGA AGCCTCAAGG 900
GAAGGGAATC GGGAAAGTGA AACCCTAACC GCATATATTG AGTTTATTTG GATGGATACC 960
AGTCCCTGTG CCACATAAAT GTTTTACATA AAAGAATGGG CTCTGAAGCC AGGCTCAGCC 1020
AATTCGTAGC TGTGTCGACT CCGGCAAGTT GCTTATCTTC TGTATTAGGA TCCCCCTCCA 1080
TAATATGGCA TAACAGTAGT GCCACCCCCA ATCTCCAGTT TAACTTCTAA GCTGGCCCCT 1140
GCCTCACCCT 1150
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