| Tag | Content |
|---|
EnhancerAtlas ID | HS183-14643 | Organism | Homo sapiens | Tissue/cell | T47D-MTVL | Coordinate | chr9:140034190-140036460 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr9:140034611-140034629 | CTTTCTTTCGTCCCTTCC | - | 6.03 | | Myog | MA0500.1 | chr9:140035299-140035310 | AACAGCTGCAG | + | 6.02 | | TP53 | MA0106.3 | chr9:140035155-140035173 | GACATGCCAGGGCATGTG | + | 7.32 | | TP53 | MA0106.3 | chr9:140035155-140035173 | GACATGCCAGGGCATGTG | - | 7.98 | | Tcf12 | MA0521.1 | chr9:140035299-140035310 | AACAGCTGCAG | + | 6.62 | | ZNF263 | MA0528.1 | chr9:140034199-140034220 | CCCTCCCCCACCTCCGCCACC | - | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGCCAGGTGC CCTCCCCCAC CTCCGCCACC CACCTCCCCT CTCCTCCATC CTGCAACCCC 60
ACACCCCCAG TTTCATTCCA TCCTTTCCGT GCCCCCTTCC TCCCTGTAAG ACACCACCCC 120
AGAGTCAGCT GGCTGCTTCC GGGAGGCCTC GTCTCACTAG GAACCAAACA CCAGGGTCTG 180
CTGGCTCCCC TATCTTGGCC TGAGACCAGT CACCTGCCAC CTTGGCTGGT CCTCAGAGGG 240
CCCCTGGGGC TCCAGGCCCT GACTGGTGTG TGTAGACGTG GGGCTGGAGT GTGTCAGTGT 300
GGGGGTGGGC ATTCCGGGTA AGAGAGTAGA AGCGCCTGTC CAGCTACATG CCCGCCCTGC 360
AGAGCTTTAA ACAGGACGGG GCCTGGGGCC ATCTTTGTTT CTGCTTCCAG GTTCTCCTGC 420
CCTTTCTTTC GTCCCTTCCC CCTACCGATG GGTCCGCCTG GGAAGAGAAA TGGCTCAGGT 480
GCCACGGCAG GACGCTTTGT GGGGGTGGGA GTGGGGGTGC ACACGCGAGA GGCATCAGGG 540
CATGGGAGCT GTCGGCAGCC AGCGCTGCGG GGGAGGACGT GGCTCCTGGG ATTTTGCCTG 600
TCGGAGCTGT CCGCCCCTGG GCCGAGCGCC TGCTGAATTC CAATGAGGCT GCAAGGATCT 660
GCAATGCAGC CCTTTATGTA AGAGGCAAGA CAGACATCCA GCCTAGCACC GCTCACACGT 720
GCCTACCTGA TGGACACACC ACATCTGTGG ACACACATGC TCACACTCAC ACCAAATGTT 780
ACATTAGCAC ACACTCATGC ACCTCAGCAT CACACAATCA ATTTCATATG CTCATCTGCA 840
CACATGCAGA TCCATTGACA CCTGCTCATG TGCCACACAC GGCTTGGCAT GCATTCCCAG 900
AGGCACGTGC AAACATGCAC ATTTACACAC ATGGTTCCAG TCATTCACAC GCATGTACAC 960
GAACAGACAT GCCAGGGCAT GTGATGCACA TAACCATACC CTAGCACACG CGTGAACACC 1020
TGCATGGTCA CACACGGACC TACGGGTCTT TGCCAAGCAC CTCTGGGTGC AGGCTGGAAG 1080
CAAGAGCTGG GGGAGGGAGA ACCACTTCAA ACAGCTGCAG CTGCAGGGCC CACACCAGAG 1140
TTTTCTCAGA AATCCTCCCT CCCCACTTCA CAAGCCACCC CCGTGCCCCA GCCCAGGACA 1200
CCATGGGATG GGACTGGGGG GATGCATCTG TAGCCAGTGG CTGCAGTCAC ATATTCCATC 1260
TGGGACTGGG GAGGGACACG GAAGGTGGAC TCAGGAAATC CAGGAGGGGC CATTCCTGGG 1320
GAATTGCTTC AACTCACGCC CATGTTGCTG TCTGTCTGTG GGCATGGCCT CTGCAGCAAA 1380
GGCAATGCCT GCAGCTACCA CTCACGGAAC ACACCCCCGG CCAGGTACTG TCCTGCCACG 1440
TGGGGCCATG CAGTGCACGC CCCCATTCGC CAAAGCTCTA AGAGGCACAG GCAGACTTGG 1500
GGACAGACGC AGGTCCTTGC TGTGTGAAGG TGGTGTGGAC CACCAGCTGC CTGCCTCCCT 1560
GCCTTGGGAG GCTGGGGAGA GAGGGAGGCA TCAGCTCCAG GGGGCTGAGC CGCTGGCTTT 1620
AGATCTGCCC CATGGGGCCT TGGTCATGGG CAGGAAGGCT GGGCTGCACC CCCAATGCCT 1680
CCCTTCCCTT CCTTGAGGAT GAGGCCAGCA CTCAAAGTAA GGGCTTGGTG TTGTTCAGAC 1740
AGAGCCCGTC ACAGGCCCTG CCCCTGGAGA CACCAGCAAA AGGGATCTCG GCCTCTTTGG 1800
CAGCTCCTAG CTGCTTCCCC CTGAAGTCCG GTACCACCCT TCAGAGCTGC CCGCCCTGTC 1860
TCGGGATGTG GGCTGGCCCC ACCCCTGGCC CATCAGGAAG GACGGGTGGG TTCTGAGAAT 1920
CAAGGCCATC ATGATGCAGG ACCAGCCATC CTCCCCGGTC CACCTTGGGT GCGTCCCGTG 1980
CTCCAGGCCC CCAGGACATC CCAAGGGCAG TCCTTCACCT GGCCCTTGAG CACAACACCT 2040
GCAGGGCCCT AGTCAGCAGT GTGAGAGGAG TGAGGGGAGG TCCGGGTGGG GTCTCCCTCC 2100
CCTGCCCTGT GGGCATGTGT GCATCTGGGC CTGGGCATGT AGCATGTACC CGAATCATGC 2160
CCCCAGCCCC CCTTAGCCTG CTGGGTTCAG CCCCTGCTGC TTCCAGATCT CAGCCTCTAA 2220
CCCAGTGCCT GGCTCACCCC TGACTCAAGC TGATCATGTC TCCTGTGTCC 2270
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